Name: rs33999296
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs33999296

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr9:14277345-14277369 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(CA)₉ / del(CA)₆ / del(CA)₅ / d…
del(CA)₉ / del(CA)₆ / del(CA)₅ / del(CA)₄ / del(CA)₃ / delCACA / delCA / dupCA / dupCACA / dup(CA)₃ / dup(CA)₄ / dup(CA)₅ / dup(CA)₆
Variation Type: Indel Insertion and Deletion
Frequency: dup(CA)₅=0.000382 (101/264690, TOPMED)
(AC)₁₂A=0.2139 (1071/5008, 1000G)
dupCACA=0.0475 (214/4502, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NFIB : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	4502	ACACACACACACACACACACACACA=0.0422	ACACACA=0.0000, ACACACACACACA=0.0000, ACACACACACACACA=0.0000, ACACACACACACACACA=0.0002, ACACACACACACACACACA=0.0000, ACACACACACACACACACACA=0.0000, ACACACACACACACACACACACA=0.0073, ACACACACACACACACACACACACACA=0.8969, ACACACACACACACACACACACACACACA=0.0475, ACACACACACACACACACACACACACACACA=0.0056, ACACACACACACACACACACACACACACACACACA=0.0002, ACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACACA=0.0000	0.900296	0.001481	0.098223	1
European	Sub	4468	ACACACACACACACACACACACACA=0.0367	ACACACA=0.0000, ACACACACACACA=0.0000, ACACACACACACACA=0.0000, ACACACACACACACACA=0.0002, ACACACACACACACACACA=0.0000, ACACACACACACACACACACA=0.0000, ACACACACACACACACACACACA=0.0074, ACACACACACACACACACACACACACA=0.9020, ACACACACACACACACACACACACACACA=0.0479, ACACACACACACACACACACACACACACACA=0.0056, ACACACACACACACACACACACACACACACACACA=0.0002, ACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACACA=0.0000	0.900099	0.001484	0.098417	1
African	Sub	20	ACACACACACACACACACACACACA=1.00	ACACACA=0.00, ACACACACACACA=0.00, ACACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACA=0.00	0	0	0	N/A
African Others	Sub	0	ACACACACACACACACACACACACA=0	ACACACA=0, ACACACACACACA=0, ACACACACACACACA=0, ACACACACACACACACA=0, ACACACACACACACACACA=0, ACACACACACACACACACACA=0, ACACACACACACACACACACACA=0, ACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACACACACACA=0	0	0	0	N/A
African American	Sub	20	ACACACACACACACACACACACACA=1.00	ACACACA=0.00, ACACACACACACA=0.00, ACACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACA=0.00	0	0	0	N/A
Asian	Sub	0	ACACACACACACACACACACACACA=0	ACACACA=0, ACACACACACACA=0, ACACACACACACACA=0, ACACACACACACACACA=0, ACACACACACACACACACA=0, ACACACACACACACACACACA=0, ACACACACACACACACACACACA=0, ACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACACACACACA=0	0	0	0	N/A
East Asian	Sub	0	ACACACACACACACACACACACACA=0	ACACACA=0, ACACACACACACA=0, ACACACACACACACA=0, ACACACACACACACACA=0, ACACACACACACACACACA=0, ACACACACACACACACACACA=0, ACACACACACACACACACACACA=0, ACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACACACACACA=0	0	0	0	N/A
Other Asian	Sub	0	ACACACACACACACACACACACACA=0	ACACACA=0, ACACACACACACA=0, ACACACACACACACA=0, ACACACACACACACACA=0, ACACACACACACACACACA=0, ACACACACACACACACACACA=0, ACACACACACACACACACACACA=0, ACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACACACACACA=0	0	0	0	N/A
Latin American 1	Sub	0	ACACACACACACACACACACACACA=0	ACACACA=0, ACACACACACACA=0, ACACACACACACACA=0, ACACACACACACACACA=0, ACACACACACACACACACA=0, ACACACACACACACACACACA=0, ACACACACACACACACACACACA=0, ACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACACACACACA=0	0	0	0	N/A
Latin American 2	Sub	2	ACACACACACACACACACACACACA=1.0	ACACACA=0.0, ACACACACACACA=0.0, ACACACACACACACA=0.0, ACACACACACACACACA=0.0, ACACACACACACACACACA=0.0, ACACACACACACACACACACA=0.0, ACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACACACACA=0.0	0	0	0	N/A
South Asian	Sub	2	ACACACACACACACACACACACACA=1.0	ACACACA=0.0, ACACACACACACA=0.0, ACACACACACACACA=0.0, ACACACACACACACACA=0.0, ACACACACACACACACACA=0.0, ACACACACACACACACACACA=0.0, ACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACACACACA=0.0	0	0	0	N/A
Other	Sub	10	ACACACACACACACACACACACACA=0.2	ACACACA=0.0, ACACACACACACA=0.0, ACACACACACACACA=0.0, ACACACACACACACACA=0.0, ACACACACACACACACACA=0.0, ACACACACACACACACACACA=0.0, ACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACA=0.8, ACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACACACACA=0.0	1.0	0.0	0.0	N/A

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	- No frequency provided	dup(CA)₅=0.000382
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupCA=0.7861
1000Genomes	African	Sub	1322	- No frequency provided	dupCA=0.7481
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupCA=0.8006
1000Genomes	Europe	Sub	1006	- No frequency provided	dupCA=0.8072
1000Genomes	South Asian	Sub	978	- No frequency provided	dupCA=0.818
1000Genomes	American	Sub	694	- No frequency provided	dupCA=0.762
Allele Frequency Aggregator	Total	Global	4502	(AC)₁₂A=0.0422	del(CA)₉=0.0000, del(CA)₆=0.0000, del(CA)₅=0.0000, del(CA)₄=0.0002, del(CA)₃=0.0000, delCACA=0.0000, delCA=0.0073, dupCA=0.8969, dupCACA=0.0475, dup(CA)₃=0.0056, dup(CA)₄=0.0000, dup(CA)₅=0.0002, dup(CA)₆=0.0000
Allele Frequency Aggregator	European	Sub	4468	(AC)₁₂A=0.0367	del(CA)₉=0.0000, del(CA)₆=0.0000, del(CA)₅=0.0000, del(CA)₄=0.0002, del(CA)₃=0.0000, delCACA=0.0000, delCA=0.0074, dupCA=0.9020, dupCACA=0.0479, dup(CA)₃=0.0056, dup(CA)₄=0.0000, dup(CA)₅=0.0002, dup(CA)₆=0.0000
Allele Frequency Aggregator	African	Sub	20	(AC)₁₂A=1.00	del(CA)₉=0.00, del(CA)₆=0.00, del(CA)₅=0.00, del(CA)₄=0.00, del(CA)₃=0.00, delCACA=0.00, delCA=0.00, dupCA=0.00, dupCACA=0.00, dup(CA)₃=0.00, dup(CA)₄=0.00, dup(CA)₅=0.00, dup(CA)₆=0.00
Allele Frequency Aggregator	Other	Sub	10	(AC)₁₂A=0.2	del(CA)₉=0.0, del(CA)₆=0.0, del(CA)₅=0.0, del(CA)₄=0.0, del(CA)₃=0.0, delCACA=0.0, delCA=0.0, dupCA=0.8, dupCACA=0.0, dup(CA)₃=0.0, dup(CA)₄=0.0, dup(CA)₅=0.0, dup(CA)₆=0.0
Allele Frequency Aggregator	Latin American 2	Sub	2	(AC)₁₂A=1.0	del(CA)₉=0.0, del(CA)₆=0.0, del(CA)₅=0.0, del(CA)₄=0.0, del(CA)₃=0.0, delCACA=0.0, delCA=0.0, dupCA=0.0, dupCACA=0.0, dup(CA)₃=0.0, dup(CA)₄=0.0, dup(CA)₅=0.0, dup(CA)₆=0.0
Allele Frequency Aggregator	South Asian	Sub	2	(AC)₁₂A=1.0	del(CA)₉=0.0, del(CA)₆=0.0, del(CA)₅=0.0, del(CA)₄=0.0, del(CA)₃=0.0, delCACA=0.0, delCA=0.0, dupCA=0.0, dupCACA=0.0, dup(CA)₃=0.0, dup(CA)₄=0.0, dup(CA)₅=0.0, dup(CA)₆=0.0
Allele Frequency Aggregator	Latin American 1	Sub	0	(AC)₁₂A=0	del(CA)₉=0, del(CA)₆=0, del(CA)₅=0, del(CA)₄=0, del(CA)₃=0, delCACA=0, delCA=0, dupCA=0, dupCACA=0, dup(CA)₃=0, dup(CA)₄=0, dup(CA)₅=0, dup(CA)₆=0
Allele Frequency Aggregator	Asian	Sub	0	(AC)₁₂A=0	del(CA)₉=0, del(CA)₆=0, del(CA)₅=0, del(CA)₄=0, del(CA)₃=0, delCACA=0, delCA=0, dupCA=0, dupCACA=0, dup(CA)₃=0, dup(CA)₄=0, dup(CA)₅=0, dup(CA)₆=0

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 9	NC_000009.12:g.14277346CA[3]
GRCh38.p14 chr 9	NC_000009.12:g.14277346CA[6]
GRCh38.p14 chr 9	NC_000009.12:g.14277346CA[7]
GRCh38.p14 chr 9	NC_000009.12:g.14277346CA[8]
GRCh38.p14 chr 9	NC_000009.12:g.14277346CA[9]
GRCh38.p14 chr 9	NC_000009.12:g.14277346CA[10]
GRCh38.p14 chr 9	NC_000009.12:g.14277346CA[11]
GRCh38.p14 chr 9	NC_000009.12:g.14277346CA[13]
GRCh38.p14 chr 9	NC_000009.12:g.14277346CA[14]
GRCh38.p14 chr 9	NC_000009.12:g.14277346CA[15]
GRCh38.p14 chr 9	NC_000009.12:g.14277346CA[16]
GRCh38.p14 chr 9	NC_000009.12:g.14277346CA[17]
GRCh38.p14 chr 9	NC_000009.12:g.14277346CA[18]
GRCh37.p13 chr 9	NC_000009.11:g.14277345CA[3]
GRCh37.p13 chr 9	NC_000009.11:g.14277345CA[6]
GRCh37.p13 chr 9	NC_000009.11:g.14277345CA[7]
GRCh37.p13 chr 9	NC_000009.11:g.14277345CA[8]
GRCh37.p13 chr 9	NC_000009.11:g.14277345CA[9]
GRCh37.p13 chr 9	NC_000009.11:g.14277345CA[10]
GRCh37.p13 chr 9	NC_000009.11:g.14277345CA[11]
GRCh37.p13 chr 9	NC_000009.11:g.14277345CA[13]
GRCh37.p13 chr 9	NC_000009.11:g.14277345CA[14]
GRCh37.p13 chr 9	NC_000009.11:g.14277345CA[15]
GRCh37.p13 chr 9	NC_000009.11:g.14277345CA[16]
GRCh37.p13 chr 9	NC_000009.11:g.14277345CA[17]
GRCh37.p13 chr 9	NC_000009.11:g.14277345CA[18]

Gene: NFIB, nuclear factor I B (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NFIB transcript variant 1	NM_001190737.2:c.562+2962… NM_001190737.2:c.562+29621GT[3]	N/A	Intron Variant
NFIB transcript variant 2	NM_001190738.2:c.640+2962… NM_001190738.2:c.640+29621GT[3]	N/A	Intron Variant
NFIB transcript variant 5	NM_001369458.1:c.628+2962… NM_001369458.1:c.628+29621GT[3]	N/A	Intron Variant
NFIB transcript variant 6	NM_001369459.1:c.628+2962… NM_001369459.1:c.628+29621GT[3]	N/A	Intron Variant
NFIB transcript variant 7	NM_001369460.1:c.550+2962… NM_001369460.1:c.550+29621GT[3]	N/A	Intron Variant
NFIB transcript variant 8	NM_001369461.1:c.562+2962… NM_001369461.1:c.562+29621GT[3]	N/A	Intron Variant
NFIB transcript variant 9	NM_001369462.1:c.628+2962… NM_001369462.1:c.628+29621GT[3]	N/A	Intron Variant
NFIB transcript variant 10	NM_001369463.1:c.550+2962… NM_001369463.1:c.550+29621GT[3]	N/A	Intron Variant
NFIB transcript variant 11	NM_001369464.1:c.562+2962… NM_001369464.1:c.562+29621GT[3]	N/A	Intron Variant
NFIB transcript variant 12	NM_001369465.1:c.535+2962… NM_001369465.1:c.535+29621GT[3]	N/A	Intron Variant
NFIB transcript variant 13	NM_001369466.1:c.550+2962… NM_001369466.1:c.550+29621GT[3]	N/A	Intron Variant
NFIB transcript variant 14	NM_001369467.1:c.535+2962… NM_001369467.1:c.535+29621GT[3]	N/A	Intron Variant
NFIB transcript variant 15	NM_001369468.1:c.628+2962… NM_001369468.1:c.628+29621GT[3]	N/A	Intron Variant
NFIB transcript variant 16	NM_001369469.1:c.418+2962… NM_001369469.1:c.418+29621GT[3]	N/A	Intron Variant
NFIB transcript variant 17	NM_001369470.1:c.325+2984… NM_001369470.1:c.325+29846GT[3]	N/A	Intron Variant
NFIB transcript variant 18	NM_001369471.1:c.562+2962… NM_001369471.1:c.562+29621GT[3]	N/A	Intron Variant
NFIB transcript variant 19	NM_001369472.1:c.550+2962… NM_001369472.1:c.550+29621GT[3]	N/A	Intron Variant
NFIB transcript variant 20	NM_001369473.1:c.550+2962… NM_001369473.1:c.550+29621GT[3]	N/A	Intron Variant
NFIB transcript variant 21	NM_001369474.1:c.547+2962… NM_001369474.1:c.547+29621GT[3]	N/A	Intron Variant
NFIB transcript variant 22	NM_001369475.1:c.337+2984… NM_001369475.1:c.337+29846GT[3]	N/A	Intron Variant
NFIB transcript variant 23	NM_001369476.1:c.535+2962… NM_001369476.1:c.535+29621GT[3]	N/A	Intron Variant
NFIB transcript variant 24	NM_001369477.1:c.562+2962… NM_001369477.1:c.562+29621GT[3]	N/A	Intron Variant
NFIB transcript variant 25	NM_001369478.1:c.325+2984… NM_001369478.1:c.325+29846GT[3]	N/A	Intron Variant
NFIB transcript variant 26	NM_001369479.1:c.25+22818… NM_001369479.1:c.25+22818GT[3]	N/A	Intron Variant
NFIB transcript variant 27	NM_001369480.1:c.25+22818… NM_001369480.1:c.25+22818GT[3]	N/A	Intron Variant
NFIB transcript variant 3	NM_005596.3:c.562+29621GT… NM_005596.3:c.562+29621GT[3]	N/A	Intron Variant
NFIB transcript variant 4	NM_001282787.2:c.	N/A	Genic Upstream Transcript Variant
NFIB transcript variant 28	NM_001369481.1:c.	N/A	Genic Downstream Transcript Variant
NFIB transcript variant 29	NR_161382.1:n.	N/A	Intron Variant
NFIB transcript variant 30	NR_161383.1:n.	N/A	Intron Variant
NFIB transcript variant 31	NR_161384.1:n.	N/A	Intron Variant
NFIB transcript variant 32	NR_161385.1:n.	N/A	Genic Upstream Transcript Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(AC)₁₂A=	del(CA)₉	del(CA)₆	del(CA)₅	del(CA)₄	del(CA)₃	delCACA	delCA	dupCA	dupCACA	dup(CA)₃	dup(CA)₄	dup(CA)₅	dup(CA)₆
GRCh38.p14 chr 9	NC_000009.12:g.14277345_14277369=	NC_000009.12:g.14277346CA[3]	NC_000009.12:g.14277346CA[6]	NC_000009.12:g.14277346CA[7]	NC_000009.12:g.14277346CA[8]	NC_000009.12:g.14277346CA[9]	NC_000009.12:g.14277346CA[10]	NC_000009.12:g.14277346CA[11]	NC_000009.12:g.14277346CA[13]	NC_000009.12:g.14277346CA[14]	NC_000009.12:g.14277346CA[15]	NC_000009.12:g.14277346CA[16]	NC_000009.12:g.14277346CA[17]	NC_000009.12:g.14277346CA[18]
GRCh37.p13 chr 9	NC_000009.11:g.14277344_14277368=	NC_000009.11:g.14277345CA[3]	NC_000009.11:g.14277345CA[6]	NC_000009.11:g.14277345CA[7]	NC_000009.11:g.14277345CA[8]	NC_000009.11:g.14277345CA[9]	NC_000009.11:g.14277345CA[10]	NC_000009.11:g.14277345CA[11]	NC_000009.11:g.14277345CA[13]	NC_000009.11:g.14277345CA[14]	NC_000009.11:g.14277345CA[15]	NC_000009.11:g.14277345CA[16]	NC_000009.11:g.14277345CA[17]	NC_000009.11:g.14277345CA[18]
NFIB transcript variant 1	NM_001190737.1:c.562+29644=	NM_001190737.1:c.562+29621GT[3]	NM_001190737.1:c.562+29621GT[6]	NM_001190737.1:c.562+29621GT[7]	NM_001190737.1:c.562+29621GT[8]	NM_001190737.1:c.562+29621GT[9]	NM_001190737.1:c.562+29621GT[10]	NM_001190737.1:c.562+29621GT[11]	NM_001190737.1:c.562+29621GT[13]	NM_001190737.1:c.562+29621GT[14]	NM_001190737.1:c.562+29621GT[15]	NM_001190737.1:c.562+29621GT[16]	NM_001190737.1:c.562+29621GT[17]	NM_001190737.1:c.562+29621GT[18]
NFIB transcript variant 1	NM_001190737.2:c.562+29644=	NM_001190737.2:c.562+29621GT[3]	NM_001190737.2:c.562+29621GT[6]	NM_001190737.2:c.562+29621GT[7]	NM_001190737.2:c.562+29621GT[8]	NM_001190737.2:c.562+29621GT[9]	NM_001190737.2:c.562+29621GT[10]	NM_001190737.2:c.562+29621GT[11]	NM_001190737.2:c.562+29621GT[13]	NM_001190737.2:c.562+29621GT[14]	NM_001190737.2:c.562+29621GT[15]	NM_001190737.2:c.562+29621GT[16]	NM_001190737.2:c.562+29621GT[17]	NM_001190737.2:c.562+29621GT[18]
NFIB transcript variant 2	NM_001190738.1:c.640+29644=	NM_001190738.1:c.640+29621GT[3]	NM_001190738.1:c.640+29621GT[6]	NM_001190738.1:c.640+29621GT[7]	NM_001190738.1:c.640+29621GT[8]	NM_001190738.1:c.640+29621GT[9]	NM_001190738.1:c.640+29621GT[10]	NM_001190738.1:c.640+29621GT[11]	NM_001190738.1:c.640+29621GT[13]	NM_001190738.1:c.640+29621GT[14]	NM_001190738.1:c.640+29621GT[15]	NM_001190738.1:c.640+29621GT[16]	NM_001190738.1:c.640+29621GT[17]	NM_001190738.1:c.640+29621GT[18]
NFIB transcript variant 2	NM_001190738.2:c.640+29644=	NM_001190738.2:c.640+29621GT[3]	NM_001190738.2:c.640+29621GT[6]	NM_001190738.2:c.640+29621GT[7]	NM_001190738.2:c.640+29621GT[8]	NM_001190738.2:c.640+29621GT[9]	NM_001190738.2:c.640+29621GT[10]	NM_001190738.2:c.640+29621GT[11]	NM_001190738.2:c.640+29621GT[13]	NM_001190738.2:c.640+29621GT[14]	NM_001190738.2:c.640+29621GT[15]	NM_001190738.2:c.640+29621GT[16]	NM_001190738.2:c.640+29621GT[17]	NM_001190738.2:c.640+29621GT[18]
NFIB transcript variant 5	NM_001369458.1:c.628+29644=	NM_001369458.1:c.628+29621GT[3]	NM_001369458.1:c.628+29621GT[6]	NM_001369458.1:c.628+29621GT[7]	NM_001369458.1:c.628+29621GT[8]	NM_001369458.1:c.628+29621GT[9]	NM_001369458.1:c.628+29621GT[10]	NM_001369458.1:c.628+29621GT[11]	NM_001369458.1:c.628+29621GT[13]	NM_001369458.1:c.628+29621GT[14]	NM_001369458.1:c.628+29621GT[15]	NM_001369458.1:c.628+29621GT[16]	NM_001369458.1:c.628+29621GT[17]	NM_001369458.1:c.628+29621GT[18]
NFIB transcript variant 6	NM_001369459.1:c.628+29644=	NM_001369459.1:c.628+29621GT[3]	NM_001369459.1:c.628+29621GT[6]	NM_001369459.1:c.628+29621GT[7]	NM_001369459.1:c.628+29621GT[8]	NM_001369459.1:c.628+29621GT[9]	NM_001369459.1:c.628+29621GT[10]	NM_001369459.1:c.628+29621GT[11]	NM_001369459.1:c.628+29621GT[13]	NM_001369459.1:c.628+29621GT[14]	NM_001369459.1:c.628+29621GT[15]	NM_001369459.1:c.628+29621GT[16]	NM_001369459.1:c.628+29621GT[17]	NM_001369459.1:c.628+29621GT[18]
NFIB transcript variant 7	NM_001369460.1:c.550+29644=	NM_001369460.1:c.550+29621GT[3]	NM_001369460.1:c.550+29621GT[6]	NM_001369460.1:c.550+29621GT[7]	NM_001369460.1:c.550+29621GT[8]	NM_001369460.1:c.550+29621GT[9]	NM_001369460.1:c.550+29621GT[10]	NM_001369460.1:c.550+29621GT[11]	NM_001369460.1:c.550+29621GT[13]	NM_001369460.1:c.550+29621GT[14]	NM_001369460.1:c.550+29621GT[15]	NM_001369460.1:c.550+29621GT[16]	NM_001369460.1:c.550+29621GT[17]	NM_001369460.1:c.550+29621GT[18]
NFIB transcript variant 8	NM_001369461.1:c.562+29644=	NM_001369461.1:c.562+29621GT[3]	NM_001369461.1:c.562+29621GT[6]	NM_001369461.1:c.562+29621GT[7]	NM_001369461.1:c.562+29621GT[8]	NM_001369461.1:c.562+29621GT[9]	NM_001369461.1:c.562+29621GT[10]	NM_001369461.1:c.562+29621GT[11]	NM_001369461.1:c.562+29621GT[13]	NM_001369461.1:c.562+29621GT[14]	NM_001369461.1:c.562+29621GT[15]	NM_001369461.1:c.562+29621GT[16]	NM_001369461.1:c.562+29621GT[17]	NM_001369461.1:c.562+29621GT[18]
NFIB transcript variant 9	NM_001369462.1:c.628+29644=	NM_001369462.1:c.628+29621GT[3]	NM_001369462.1:c.628+29621GT[6]	NM_001369462.1:c.628+29621GT[7]	NM_001369462.1:c.628+29621GT[8]	NM_001369462.1:c.628+29621GT[9]	NM_001369462.1:c.628+29621GT[10]	NM_001369462.1:c.628+29621GT[11]	NM_001369462.1:c.628+29621GT[13]	NM_001369462.1:c.628+29621GT[14]	NM_001369462.1:c.628+29621GT[15]	NM_001369462.1:c.628+29621GT[16]	NM_001369462.1:c.628+29621GT[17]	NM_001369462.1:c.628+29621GT[18]
NFIB transcript variant 10	NM_001369463.1:c.550+29644=	NM_001369463.1:c.550+29621GT[3]	NM_001369463.1:c.550+29621GT[6]	NM_001369463.1:c.550+29621GT[7]	NM_001369463.1:c.550+29621GT[8]	NM_001369463.1:c.550+29621GT[9]	NM_001369463.1:c.550+29621GT[10]	NM_001369463.1:c.550+29621GT[11]	NM_001369463.1:c.550+29621GT[13]	NM_001369463.1:c.550+29621GT[14]	NM_001369463.1:c.550+29621GT[15]	NM_001369463.1:c.550+29621GT[16]	NM_001369463.1:c.550+29621GT[17]	NM_001369463.1:c.550+29621GT[18]
NFIB transcript variant 11	NM_001369464.1:c.562+29644=	NM_001369464.1:c.562+29621GT[3]	NM_001369464.1:c.562+29621GT[6]	NM_001369464.1:c.562+29621GT[7]	NM_001369464.1:c.562+29621GT[8]	NM_001369464.1:c.562+29621GT[9]	NM_001369464.1:c.562+29621GT[10]	NM_001369464.1:c.562+29621GT[11]	NM_001369464.1:c.562+29621GT[13]	NM_001369464.1:c.562+29621GT[14]	NM_001369464.1:c.562+29621GT[15]	NM_001369464.1:c.562+29621GT[16]	NM_001369464.1:c.562+29621GT[17]	NM_001369464.1:c.562+29621GT[18]
NFIB transcript variant 12	NM_001369465.1:c.535+29644=	NM_001369465.1:c.535+29621GT[3]	NM_001369465.1:c.535+29621GT[6]	NM_001369465.1:c.535+29621GT[7]	NM_001369465.1:c.535+29621GT[8]	NM_001369465.1:c.535+29621GT[9]	NM_001369465.1:c.535+29621GT[10]	NM_001369465.1:c.535+29621GT[11]	NM_001369465.1:c.535+29621GT[13]	NM_001369465.1:c.535+29621GT[14]	NM_001369465.1:c.535+29621GT[15]	NM_001369465.1:c.535+29621GT[16]	NM_001369465.1:c.535+29621GT[17]	NM_001369465.1:c.535+29621GT[18]
NFIB transcript variant 13	NM_001369466.1:c.550+29644=	NM_001369466.1:c.550+29621GT[3]	NM_001369466.1:c.550+29621GT[6]	NM_001369466.1:c.550+29621GT[7]	NM_001369466.1:c.550+29621GT[8]	NM_001369466.1:c.550+29621GT[9]	NM_001369466.1:c.550+29621GT[10]	NM_001369466.1:c.550+29621GT[11]	NM_001369466.1:c.550+29621GT[13]	NM_001369466.1:c.550+29621GT[14]	NM_001369466.1:c.550+29621GT[15]	NM_001369466.1:c.550+29621GT[16]	NM_001369466.1:c.550+29621GT[17]	NM_001369466.1:c.550+29621GT[18]
NFIB transcript variant 14	NM_001369467.1:c.535+29644=	NM_001369467.1:c.535+29621GT[3]	NM_001369467.1:c.535+29621GT[6]	NM_001369467.1:c.535+29621GT[7]	NM_001369467.1:c.535+29621GT[8]	NM_001369467.1:c.535+29621GT[9]	NM_001369467.1:c.535+29621GT[10]	NM_001369467.1:c.535+29621GT[11]	NM_001369467.1:c.535+29621GT[13]	NM_001369467.1:c.535+29621GT[14]	NM_001369467.1:c.535+29621GT[15]	NM_001369467.1:c.535+29621GT[16]	NM_001369467.1:c.535+29621GT[17]	NM_001369467.1:c.535+29621GT[18]
NFIB transcript variant 15	NM_001369468.1:c.628+29644=	NM_001369468.1:c.628+29621GT[3]	NM_001369468.1:c.628+29621GT[6]	NM_001369468.1:c.628+29621GT[7]	NM_001369468.1:c.628+29621GT[8]	NM_001369468.1:c.628+29621GT[9]	NM_001369468.1:c.628+29621GT[10]	NM_001369468.1:c.628+29621GT[11]	NM_001369468.1:c.628+29621GT[13]	NM_001369468.1:c.628+29621GT[14]	NM_001369468.1:c.628+29621GT[15]	NM_001369468.1:c.628+29621GT[16]	NM_001369468.1:c.628+29621GT[17]	NM_001369468.1:c.628+29621GT[18]
NFIB transcript variant 16	NM_001369469.1:c.418+29644=	NM_001369469.1:c.418+29621GT[3]	NM_001369469.1:c.418+29621GT[6]	NM_001369469.1:c.418+29621GT[7]	NM_001369469.1:c.418+29621GT[8]	NM_001369469.1:c.418+29621GT[9]	NM_001369469.1:c.418+29621GT[10]	NM_001369469.1:c.418+29621GT[11]	NM_001369469.1:c.418+29621GT[13]	NM_001369469.1:c.418+29621GT[14]	NM_001369469.1:c.418+29621GT[15]	NM_001369469.1:c.418+29621GT[16]	NM_001369469.1:c.418+29621GT[17]	NM_001369469.1:c.418+29621GT[18]
NFIB transcript variant 17	NM_001369470.1:c.325+29869=	NM_001369470.1:c.325+29846GT[3]	NM_001369470.1:c.325+29846GT[6]	NM_001369470.1:c.325+29846GT[7]	NM_001369470.1:c.325+29846GT[8]	NM_001369470.1:c.325+29846GT[9]	NM_001369470.1:c.325+29846GT[10]	NM_001369470.1:c.325+29846GT[11]	NM_001369470.1:c.325+29846GT[13]	NM_001369470.1:c.325+29846GT[14]	NM_001369470.1:c.325+29846GT[15]	NM_001369470.1:c.325+29846GT[16]	NM_001369470.1:c.325+29846GT[17]	NM_001369470.1:c.325+29846GT[18]
NFIB transcript variant 18	NM_001369471.1:c.562+29644=	NM_001369471.1:c.562+29621GT[3]	NM_001369471.1:c.562+29621GT[6]	NM_001369471.1:c.562+29621GT[7]	NM_001369471.1:c.562+29621GT[8]	NM_001369471.1:c.562+29621GT[9]	NM_001369471.1:c.562+29621GT[10]	NM_001369471.1:c.562+29621GT[11]	NM_001369471.1:c.562+29621GT[13]	NM_001369471.1:c.562+29621GT[14]	NM_001369471.1:c.562+29621GT[15]	NM_001369471.1:c.562+29621GT[16]	NM_001369471.1:c.562+29621GT[17]	NM_001369471.1:c.562+29621GT[18]
NFIB transcript variant 19	NM_001369472.1:c.550+29644=	NM_001369472.1:c.550+29621GT[3]	NM_001369472.1:c.550+29621GT[6]	NM_001369472.1:c.550+29621GT[7]	NM_001369472.1:c.550+29621GT[8]	NM_001369472.1:c.550+29621GT[9]	NM_001369472.1:c.550+29621GT[10]	NM_001369472.1:c.550+29621GT[11]	NM_001369472.1:c.550+29621GT[13]	NM_001369472.1:c.550+29621GT[14]	NM_001369472.1:c.550+29621GT[15]	NM_001369472.1:c.550+29621GT[16]	NM_001369472.1:c.550+29621GT[17]	NM_001369472.1:c.550+29621GT[18]
NFIB transcript variant 20	NM_001369473.1:c.550+29644=	NM_001369473.1:c.550+29621GT[3]	NM_001369473.1:c.550+29621GT[6]	NM_001369473.1:c.550+29621GT[7]	NM_001369473.1:c.550+29621GT[8]	NM_001369473.1:c.550+29621GT[9]	NM_001369473.1:c.550+29621GT[10]	NM_001369473.1:c.550+29621GT[11]	NM_001369473.1:c.550+29621GT[13]	NM_001369473.1:c.550+29621GT[14]	NM_001369473.1:c.550+29621GT[15]	NM_001369473.1:c.550+29621GT[16]	NM_001369473.1:c.550+29621GT[17]	NM_001369473.1:c.550+29621GT[18]
NFIB transcript variant 21	NM_001369474.1:c.547+29644=	NM_001369474.1:c.547+29621GT[3]	NM_001369474.1:c.547+29621GT[6]	NM_001369474.1:c.547+29621GT[7]	NM_001369474.1:c.547+29621GT[8]	NM_001369474.1:c.547+29621GT[9]	NM_001369474.1:c.547+29621GT[10]	NM_001369474.1:c.547+29621GT[11]	NM_001369474.1:c.547+29621GT[13]	NM_001369474.1:c.547+29621GT[14]	NM_001369474.1:c.547+29621GT[15]	NM_001369474.1:c.547+29621GT[16]	NM_001369474.1:c.547+29621GT[17]	NM_001369474.1:c.547+29621GT[18]
NFIB transcript variant 22	NM_001369475.1:c.337+29869=	NM_001369475.1:c.337+29846GT[3]	NM_001369475.1:c.337+29846GT[6]	NM_001369475.1:c.337+29846GT[7]	NM_001369475.1:c.337+29846GT[8]	NM_001369475.1:c.337+29846GT[9]	NM_001369475.1:c.337+29846GT[10]	NM_001369475.1:c.337+29846GT[11]	NM_001369475.1:c.337+29846GT[13]	NM_001369475.1:c.337+29846GT[14]	NM_001369475.1:c.337+29846GT[15]	NM_001369475.1:c.337+29846GT[16]	NM_001369475.1:c.337+29846GT[17]	NM_001369475.1:c.337+29846GT[18]
NFIB transcript variant 23	NM_001369476.1:c.535+29644=	NM_001369476.1:c.535+29621GT[3]	NM_001369476.1:c.535+29621GT[6]	NM_001369476.1:c.535+29621GT[7]	NM_001369476.1:c.535+29621GT[8]	NM_001369476.1:c.535+29621GT[9]	NM_001369476.1:c.535+29621GT[10]	NM_001369476.1:c.535+29621GT[11]	NM_001369476.1:c.535+29621GT[13]	NM_001369476.1:c.535+29621GT[14]	NM_001369476.1:c.535+29621GT[15]	NM_001369476.1:c.535+29621GT[16]	NM_001369476.1:c.535+29621GT[17]	NM_001369476.1:c.535+29621GT[18]
NFIB transcript variant 24	NM_001369477.1:c.562+29644=	NM_001369477.1:c.562+29621GT[3]	NM_001369477.1:c.562+29621GT[6]	NM_001369477.1:c.562+29621GT[7]	NM_001369477.1:c.562+29621GT[8]	NM_001369477.1:c.562+29621GT[9]	NM_001369477.1:c.562+29621GT[10]	NM_001369477.1:c.562+29621GT[11]	NM_001369477.1:c.562+29621GT[13]	NM_001369477.1:c.562+29621GT[14]	NM_001369477.1:c.562+29621GT[15]	NM_001369477.1:c.562+29621GT[16]	NM_001369477.1:c.562+29621GT[17]	NM_001369477.1:c.562+29621GT[18]
NFIB transcript variant 25	NM_001369478.1:c.325+29869=	NM_001369478.1:c.325+29846GT[3]	NM_001369478.1:c.325+29846GT[6]	NM_001369478.1:c.325+29846GT[7]	NM_001369478.1:c.325+29846GT[8]	NM_001369478.1:c.325+29846GT[9]	NM_001369478.1:c.325+29846GT[10]	NM_001369478.1:c.325+29846GT[11]	NM_001369478.1:c.325+29846GT[13]	NM_001369478.1:c.325+29846GT[14]	NM_001369478.1:c.325+29846GT[15]	NM_001369478.1:c.325+29846GT[16]	NM_001369478.1:c.325+29846GT[17]	NM_001369478.1:c.325+29846GT[18]
NFIB transcript variant 26	NM_001369479.1:c.25+22841=	NM_001369479.1:c.25+22818GT[3]	NM_001369479.1:c.25+22818GT[6]	NM_001369479.1:c.25+22818GT[7]	NM_001369479.1:c.25+22818GT[8]	NM_001369479.1:c.25+22818GT[9]	NM_001369479.1:c.25+22818GT[10]	NM_001369479.1:c.25+22818GT[11]	NM_001369479.1:c.25+22818GT[13]	NM_001369479.1:c.25+22818GT[14]	NM_001369479.1:c.25+22818GT[15]	NM_001369479.1:c.25+22818GT[16]	NM_001369479.1:c.25+22818GT[17]	NM_001369479.1:c.25+22818GT[18]
NFIB transcript variant 27	NM_001369480.1:c.25+22841=	NM_001369480.1:c.25+22818GT[3]	NM_001369480.1:c.25+22818GT[6]	NM_001369480.1:c.25+22818GT[7]	NM_001369480.1:c.25+22818GT[8]	NM_001369480.1:c.25+22818GT[9]	NM_001369480.1:c.25+22818GT[10]	NM_001369480.1:c.25+22818GT[11]	NM_001369480.1:c.25+22818GT[13]	NM_001369480.1:c.25+22818GT[14]	NM_001369480.1:c.25+22818GT[15]	NM_001369480.1:c.25+22818GT[16]	NM_001369480.1:c.25+22818GT[17]	NM_001369480.1:c.25+22818GT[18]
NFIB transcript variant 3	NM_005596.3:c.562+29644=	NM_005596.3:c.562+29621GT[3]	NM_005596.3:c.562+29621GT[6]	NM_005596.3:c.562+29621GT[7]	NM_005596.3:c.562+29621GT[8]	NM_005596.3:c.562+29621GT[9]	NM_005596.3:c.562+29621GT[10]	NM_005596.3:c.562+29621GT[11]	NM_005596.3:c.562+29621GT[13]	NM_005596.3:c.562+29621GT[14]	NM_005596.3:c.562+29621GT[15]	NM_005596.3:c.562+29621GT[16]	NM_005596.3:c.562+29621GT[17]	NM_005596.3:c.562+29621GT[18]
NFIB transcript variant X1	XM_005251467.1:c.562+29644=	XM_005251467.1:c.562+29621GT[3]	XM_005251467.1:c.562+29621GT[6]	XM_005251467.1:c.562+29621GT[7]	XM_005251467.1:c.562+29621GT[8]	XM_005251467.1:c.562+29621GT[9]	XM_005251467.1:c.562+29621GT[10]	XM_005251467.1:c.562+29621GT[11]	XM_005251467.1:c.562+29621GT[13]	XM_005251467.1:c.562+29621GT[14]	XM_005251467.1:c.562+29621GT[15]	XM_005251467.1:c.562+29621GT[16]	XM_005251467.1:c.562+29621GT[17]	XM_005251467.1:c.562+29621GT[18]
NFIB transcript variant X2	XM_005251468.1:c.550+29644=	XM_005251468.1:c.550+29621GT[3]	XM_005251468.1:c.550+29621GT[6]	XM_005251468.1:c.550+29621GT[7]	XM_005251468.1:c.550+29621GT[8]	XM_005251468.1:c.550+29621GT[9]	XM_005251468.1:c.550+29621GT[10]	XM_005251468.1:c.550+29621GT[11]	XM_005251468.1:c.550+29621GT[13]	XM_005251468.1:c.550+29621GT[14]	XM_005251468.1:c.550+29621GT[15]	XM_005251468.1:c.550+29621GT[16]	XM_005251468.1:c.550+29621GT[17]	XM_005251468.1:c.550+29621GT[18]
NFIB transcript variant X4	XM_005251469.1:c.562+29644=	XM_005251469.1:c.562+29621GT[3]	XM_005251469.1:c.562+29621GT[6]	XM_005251469.1:c.562+29621GT[7]	XM_005251469.1:c.562+29621GT[8]	XM_005251469.1:c.562+29621GT[9]	XM_005251469.1:c.562+29621GT[10]	XM_005251469.1:c.562+29621GT[11]	XM_005251469.1:c.562+29621GT[13]	XM_005251469.1:c.562+29621GT[14]	XM_005251469.1:c.562+29621GT[15]	XM_005251469.1:c.562+29621GT[16]	XM_005251469.1:c.562+29621GT[17]	XM_005251469.1:c.562+29621GT[18]
NFIB transcript variant X7	XM_005251470.1:c.562+29644=	XM_005251470.1:c.562+29621GT[3]	XM_005251470.1:c.562+29621GT[6]	XM_005251470.1:c.562+29621GT[7]	XM_005251470.1:c.562+29621GT[8]	XM_005251470.1:c.562+29621GT[9]	XM_005251470.1:c.562+29621GT[10]	XM_005251470.1:c.562+29621GT[11]	XM_005251470.1:c.562+29621GT[13]	XM_005251470.1:c.562+29621GT[14]	XM_005251470.1:c.562+29621GT[15]	XM_005251470.1:c.562+29621GT[16]	XM_005251470.1:c.562+29621GT[17]	XM_005251470.1:c.562+29621GT[18]

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

72 SubSNP, 34 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss82671554	Dec 03, 2013 (138)
2	HUMANGENOME_JCVI	ss95511256	Dec 05, 2013 (138)
3	BL	ss256102516	May 09, 2011 (134)
4	GMI	ss288949012	May 04, 2012 (138)
5	1000GENOMES	ss327127034	May 09, 2011 (134)
6	1000GENOMES	ss327196897	May 09, 2011 (134)
7	1000GENOMES	ss327550352	May 09, 2011 (134)
8	LUNTER	ss551917604	Apr 25, 2013 (138)
9	LUNTER	ss552145496	Apr 25, 2013 (138)
10	LUNTER	ss553369063	Apr 25, 2013 (138)
11	BILGI_BIOE	ss666461532	Apr 25, 2013 (138)
12	1000GENOMES	ss1368173683	Aug 21, 2014 (142)
13	DDI	ss1536612186	Apr 01, 2015 (144)
14	EVA_UK10K_ALSPAC	ss1706335125	Apr 01, 2015 (144)
15	EVA_UK10K_ALSPAC	ss1706335126	Apr 01, 2015 (144)
16	EVA_UK10K_TWINSUK	ss1706335150	Apr 01, 2015 (144)
17	EVA_UK10K_TWINSUK	ss1706335153	Apr 01, 2015 (144)
18	HAMMER_LAB	ss1805891994	Sep 08, 2015 (146)
19	SWEGEN	ss3004432676	Nov 08, 2017 (151)
20	MCHAISSO	ss3065217792	Nov 08, 2017 (151)
21	MCHAISSO	ss3066239083	Nov 08, 2017 (151)
22	URBANLAB	ss3649077669	Oct 12, 2018 (152)
23	EVA_DECODE	ss3723534724	Jul 13, 2019 (153)
24	EVA_DECODE	ss3723534725	Jul 13, 2019 (153)
25	EVA_DECODE	ss3723534726	Jul 13, 2019 (153)
26	EVA_DECODE	ss3723534727	Jul 13, 2019 (153)
27	EVA_DECODE	ss3723534728	Jul 13, 2019 (153)
28	EVA_DECODE	ss3723534729	Jul 13, 2019 (153)
29	ACPOP	ss3736336406	Jul 13, 2019 (153)
30	ACPOP	ss3736336407	Jul 13, 2019 (153)
31	ACPOP	ss3736336408	Jul 13, 2019 (153)
32	PACBIO	ss3786356163	Jul 13, 2019 (153)
33	PACBIO	ss3791581043	Jul 13, 2019 (153)
34	PACBIO	ss3796462701	Jul 13, 2019 (153)
35	KHV_HUMAN_GENOMES	ss3812112382	Jul 13, 2019 (153)
36	KHV_HUMAN_GENOMES	ss3812112383	Jul 13, 2019 (153)
37	EVA	ss3831553048	Apr 26, 2020 (154)
38	EVA	ss3839291689	Apr 26, 2020 (154)
39	EVA	ss3844753972	Apr 26, 2020 (154)
40	GNOMAD	ss4198081389	Apr 26, 2021 (155)
41	GNOMAD	ss4198081390	Apr 26, 2021 (155)
42	GNOMAD	ss4198081391	Apr 26, 2021 (155)
43	GNOMAD	ss4198081392	Apr 26, 2021 (155)
44	GNOMAD	ss4198081393	Apr 26, 2021 (155)
45	GNOMAD	ss4198081394	Apr 26, 2021 (155)
46	GNOMAD	ss4198081396	Apr 26, 2021 (155)
47	GNOMAD	ss4198081397	Apr 26, 2021 (155)
48	GNOMAD	ss4198081398	Apr 26, 2021 (155)
49	GNOMAD	ss4198081399	Apr 26, 2021 (155)
50	GNOMAD	ss4198081400	Apr 26, 2021 (155)
51	GNOMAD	ss4198081401	Apr 26, 2021 (155)
52	TOPMED	ss4813657007	Apr 26, 2021 (155)
53	TOMMO_GENOMICS	ss5192216476	Apr 26, 2021 (155)
54	TOMMO_GENOMICS	ss5192216477	Apr 26, 2021 (155)
55	TOMMO_GENOMICS	ss5192216478	Apr 26, 2021 (155)
56	TOMMO_GENOMICS	ss5192216479	Apr 26, 2021 (155)
57	TOMMO_GENOMICS	ss5192216480	Apr 26, 2021 (155)
58	TOMMO_GENOMICS	ss5192216481	Apr 26, 2021 (155)
59	1000G_HIGH_COVERAGE	ss5279900015	Oct 16, 2022 (156)
60	1000G_HIGH_COVERAGE	ss5279900016	Oct 16, 2022 (156)
61	HUGCELL_USP	ss5476171678	Oct 16, 2022 (156)
62	HUGCELL_USP	ss5476171679	Oct 16, 2022 (156)
63	HUGCELL_USP	ss5476171680	Oct 16, 2022 (156)
64	HUGCELL_USP	ss5476171681	Oct 16, 2022 (156)
65	TOMMO_GENOMICS	ss5735302255	Oct 16, 2022 (156)
66	TOMMO_GENOMICS	ss5735302256	Oct 16, 2022 (156)
67	TOMMO_GENOMICS	ss5735302257	Oct 16, 2022 (156)
68	TOMMO_GENOMICS	ss5735302258	Oct 16, 2022 (156)
69	TOMMO_GENOMICS	ss5735302259	Oct 16, 2022 (156)
70	TOMMO_GENOMICS	ss5735302260	Oct 16, 2022 (156)
71	EVA	ss5828892278	Oct 16, 2022 (156)
72	EVA	ss5828892279	Oct 16, 2022 (156)
73	1000Genomes	NC_000009.11 - 14277344	Oct 12, 2018 (152)
74	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 25178687 (NC_000009.11:14277343::AC 3060/3854) Row 25178688 (NC_000009.11:14277343::ACAC 252/3854)	-	Oct 12, 2018 (152)
75	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 25178687 (NC_000009.11:14277343::AC 3060/3854) Row 25178688 (NC_000009.11:14277343::ACAC 252/3854)	-	Oct 12, 2018 (152)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 318985937 (NC_000009.12:14277344::AC 117080/137532) Row 318985938 (NC_000009.12:14277344::ACAC 10266/137464) Row 318985939 (NC_000009.12:14277344::ACACAC 767/137564)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 318985937 (NC_000009.12:14277344::AC 117080/137532) Row 318985938 (NC_000009.12:14277344::ACAC 10266/137464) Row 318985939 (NC_000009.12:14277344::ACACAC 767/137564)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 318985937 (NC_000009.12:14277344::AC 117080/137532) Row 318985938 (NC_000009.12:14277344::ACAC 10266/137464) Row 318985939 (NC_000009.12:14277344::ACACAC 767/137564)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 318985937 (NC_000009.12:14277344::AC 117080/137532) Row 318985938 (NC_000009.12:14277344::ACAC 10266/137464) Row 318985939 (NC_000009.12:14277344::ACACAC 767/137564)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 318985937 (NC_000009.12:14277344::AC 117080/137532) Row 318985938 (NC_000009.12:14277344::ACAC 10266/137464) Row 318985939 (NC_000009.12:14277344::ACACAC 767/137564)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 318985937 (NC_000009.12:14277344::AC 117080/137532) Row 318985938 (NC_000009.12:14277344::ACAC 10266/137464) Row 318985939 (NC_000009.12:14277344::ACACAC 767/137564)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 318985937 (NC_000009.12:14277344::AC 117080/137532) Row 318985938 (NC_000009.12:14277344::ACAC 10266/137464) Row 318985939 (NC_000009.12:14277344::ACACAC 767/137564)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 318985937 (NC_000009.12:14277344::AC 117080/137532) Row 318985938 (NC_000009.12:14277344::ACAC 10266/137464) Row 318985939 (NC_000009.12:14277344::ACACAC 767/137564)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 318985937 (NC_000009.12:14277344::AC 117080/137532) Row 318985938 (NC_000009.12:14277344::ACAC 10266/137464) Row 318985939 (NC_000009.12:14277344::ACACAC 767/137564)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 318985937 (NC_000009.12:14277344::AC 117080/137532) Row 318985938 (NC_000009.12:14277344::ACAC 10266/137464) Row 318985939 (NC_000009.12:14277344::ACACAC 767/137564)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 318985937 (NC_000009.12:14277344::AC 117080/137532) Row 318985938 (NC_000009.12:14277344::ACAC 10266/137464) Row 318985939 (NC_000009.12:14277344::ACACAC 767/137564)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 318985937 (NC_000009.12:14277344::AC 117080/137532) Row 318985938 (NC_000009.12:14277344::ACAC 10266/137464) Row 318985939 (NC_000009.12:14277344::ACACAC 767/137564)...	-	Apr 26, 2021 (155)
88	Northern Sweden Submission ignored due to conflicting rows: Row 9621271 (NC_000009.11:14277343::AC 555/600) Row 9621272 (NC_000009.11:14277343::ACAC 20/600) Row 9621273 (NC_000009.11:14277343:AC: 4/600)	-	Jul 13, 2019 (153)
89	Northern Sweden Submission ignored due to conflicting rows: Row 9621271 (NC_000009.11:14277343::AC 555/600) Row 9621272 (NC_000009.11:14277343::ACAC 20/600) Row 9621273 (NC_000009.11:14277343:AC: 4/600)	-	Jul 13, 2019 (153)
90	Northern Sweden Submission ignored due to conflicting rows: Row 9621271 (NC_000009.11:14277343::AC 555/600) Row 9621272 (NC_000009.11:14277343::ACAC 20/600) Row 9621273 (NC_000009.11:14277343:AC: 4/600)	-	Jul 13, 2019 (153)
91	8.3KJPN Submission ignored due to conflicting rows: Row 50185783 (NC_000009.11:14277343::AC 11147/16760) Row 50185784 (NC_000009.11:14277343::ACAC 4548/16760) Row 50185785 (NC_000009.11:14277343:AC: 42/16760)...	-	Apr 26, 2021 (155)
92	8.3KJPN Submission ignored due to conflicting rows: Row 50185783 (NC_000009.11:14277343::AC 11147/16760) Row 50185784 (NC_000009.11:14277343::ACAC 4548/16760) Row 50185785 (NC_000009.11:14277343:AC: 42/16760)...	-	Apr 26, 2021 (155)
93	8.3KJPN Submission ignored due to conflicting rows: Row 50185783 (NC_000009.11:14277343::AC 11147/16760) Row 50185784 (NC_000009.11:14277343::ACAC 4548/16760) Row 50185785 (NC_000009.11:14277343:AC: 42/16760)...	-	Apr 26, 2021 (155)
94	8.3KJPN Submission ignored due to conflicting rows: Row 50185783 (NC_000009.11:14277343::AC 11147/16760) Row 50185784 (NC_000009.11:14277343::ACAC 4548/16760) Row 50185785 (NC_000009.11:14277343:AC: 42/16760)...	-	Apr 26, 2021 (155)
95	8.3KJPN Submission ignored due to conflicting rows: Row 50185783 (NC_000009.11:14277343::AC 11147/16760) Row 50185784 (NC_000009.11:14277343::ACAC 4548/16760) Row 50185785 (NC_000009.11:14277343:AC: 42/16760)...	-	Apr 26, 2021 (155)
96	8.3KJPN Submission ignored due to conflicting rows: Row 50185783 (NC_000009.11:14277343::AC 11147/16760) Row 50185784 (NC_000009.11:14277343::ACAC 4548/16760) Row 50185785 (NC_000009.11:14277343:AC: 42/16760)...	-	Apr 26, 2021 (155)
97	14KJPN Submission ignored due to conflicting rows: Row 69139359 (NC_000009.12:14277344::AC 18801/28258) Row 69139360 (NC_000009.12:14277344::ACAC 7642/28258) Row 69139361 (NC_000009.12:14277344::ACACAC 356/28258)...	-	Oct 16, 2022 (156)
98	14KJPN Submission ignored due to conflicting rows: Row 69139359 (NC_000009.12:14277344::AC 18801/28258) Row 69139360 (NC_000009.12:14277344::ACAC 7642/28258) Row 69139361 (NC_000009.12:14277344::ACACAC 356/28258)...	-	Oct 16, 2022 (156)
99	14KJPN Submission ignored due to conflicting rows: Row 69139359 (NC_000009.12:14277344::AC 18801/28258) Row 69139360 (NC_000009.12:14277344::ACAC 7642/28258) Row 69139361 (NC_000009.12:14277344::ACACAC 356/28258)...	-	Oct 16, 2022 (156)
100	14KJPN Submission ignored due to conflicting rows: Row 69139359 (NC_000009.12:14277344::AC 18801/28258) Row 69139360 (NC_000009.12:14277344::ACAC 7642/28258) Row 69139361 (NC_000009.12:14277344::ACACAC 356/28258)...	-	Oct 16, 2022 (156)
101	14KJPN Submission ignored due to conflicting rows: Row 69139359 (NC_000009.12:14277344::AC 18801/28258) Row 69139360 (NC_000009.12:14277344::ACAC 7642/28258) Row 69139361 (NC_000009.12:14277344::ACACAC 356/28258)...	-	Oct 16, 2022 (156)
102	14KJPN Submission ignored due to conflicting rows: Row 69139359 (NC_000009.12:14277344::AC 18801/28258) Row 69139360 (NC_000009.12:14277344::ACAC 7642/28258) Row 69139361 (NC_000009.12:14277344::ACACAC 356/28258)...	-	Oct 16, 2022 (156)
103	TopMed	NC_000009.12 - 14277345	Apr 26, 2021 (155)
104	UK 10K study - Twins Submission ignored due to conflicting rows: Row 25178687 (NC_000009.11:14277343::AC 2862/3708) Row 25178688 (NC_000009.11:14277343::ACAC 250/3708)	-	Oct 12, 2018 (152)
105	UK 10K study - Twins Submission ignored due to conflicting rows: Row 25178687 (NC_000009.11:14277343::AC 2862/3708) Row 25178688 (NC_000009.11:14277343::ACAC 250/3708)	-	Oct 12, 2018 (152)
106	ALFA	NC_000009.12 - 14277345	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs58968039	May 15, 2013 (138)
rs138494949	May 11, 2012 (137)
rs140455694	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4198081401	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACAC:	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACA	(self)
4316344001	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACA	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACA	(self)
ss4198081400	NC_000009.12:14277344:ACACACACACAC:	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACA	(self)
4316344001	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACA	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACA	(self)
4316344001	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACA	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACA	(self)
ss5192216481	NC_000009.11:14277343:ACACACAC:	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACA	(self)
ss3723534729, ss4198081399	NC_000009.12:14277344:ACACACAC:	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACA	(self)
4316344001	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACA	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACA	(self)
ss4198081398	NC_000009.12:14277344:ACACAC:	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACA	(self)
4316344001	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACA	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACA	(self)
ss3004432676	NC_000009.11:14277343:ACAC:	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACA	(self)
ss4198081397	NC_000009.12:14277344:ACAC:	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACA	(self)
4316344001	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACA	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACA	(self)
ss3723534728	NC_000009.12:14277348:ACAC:	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACA	(self)
ss3736336408, ss5192216478	NC_000009.11:14277343:AC:	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss4198081396, ss5476171680, ss5735302258	NC_000009.12:14277344:AC:	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
4316344001	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACA	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss3723534727	NC_000009.12:14277350:AC:	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss256102516, ss327127034, ss327196897, ss327550352, ss551917604, ss552145496, ss553369063	NC_000009.10:14267343::AC	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
ss288949012	NC_000009.10:14267368::CA	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
45254781, ss666461532, ss1368173683, ss1536612186, ss1706335125, ss1706335150, ss1805891994, ss3736336406, ss3786356163, ss3791581043, ss3796462701, ss3831553048, ss3839291689, ss5192216476, ss5828892278	NC_000009.11:14277343::AC	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
ss3065217792, ss3066239083, ss3812112382, ss3844753972, ss4198081389, ss5279900015, ss5476171678, ss5735302255	NC_000009.12:14277344::AC	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
4316344001	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACA	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
ss3723534726	NC_000009.12:14277352::AC	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
ss3649077669	NC_000009.12:14277369::CA	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
ss82671554, ss95511256	NT_008413.18:14267368::CA	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
ss1706335126, ss1706335153, ss3736336407, ss5192216477, ss5828892279	NC_000009.11:14277343::ACAC	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACA	(self)
ss3812112383, ss4198081390, ss5279900016, ss5476171679, ss5735302256	NC_000009.12:14277344::ACAC	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACA	(self)
4316344001	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACA	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACA	(self)
ss3723534725	NC_000009.12:14277352::ACAC	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACA	(self)
ss5192216479	NC_000009.11:14277343::ACACAC	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA	(self)
ss4198081391, ss5476171681, ss5735302257	NC_000009.12:14277344::ACACAC	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA	(self)
4316344001	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA	(self)
ss3723534724	NC_000009.12:14277352::ACACAC	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA	(self)
ss4198081392, ss5735302260	NC_000009.12:14277344::ACACACAC	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACA	(self)
4316344001	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACA	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACA	(self)
ss5192216480	NC_000009.11:14277343::ACACACACAC	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACA	(self)
651034568, ss4198081393, ss4813657007, ss5735302259	NC_000009.12:14277344::ACACACACAC	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACA	(self)
4316344001	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACA	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACA	(self)
ss4198081394	NC_000009.12:14277344::ACACACACACAC	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACA	(self)
4316344001	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACA	NC_000009.12:14277344:ACACACACACAC… NC_000009.12:14277344:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACA	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs33999296

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs33999296