Name: rs34174911
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.

rs34174911

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr9:34419074-34419105 (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(CAAA)₃ / del(CAAA)₂ / delCAAA …
del(CAAA)₃ / del(CAAA)₂ / delCAAA / dupCAAA / dup(CAAA)₂ / dup(CAAA)₃ / dup(CAAA)₄
Variation Type: Indel Insertion and Deletion
Frequency: del(CAAA)₃=0.00000 (0/11882, ALFA)
del(CAAA)₂=0.00000 (0/11882, ALFA)
delCAAA=0.00000 (0/11882, ALFA) (+ 6 more)
dupCAAA=0.00000 (0/11882, ALFA)
dup(CAAA)₂=0.00000 (0/11882, ALFA)
dup(CAAA)₃=0.00000 (0/11882, ALFA)
delCAAA=0.0407 (204/5008, 1000G)
delCAAA=0.005 (1/216, Vietnamese)
dupCAAA=0.10 (4/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: FAM219A : Intron Variant
LOC124902145 : 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	HWEP
Total	Global	11882	CAAACAAACAAACAAACAAACAAACAAACAAA=1.00000	CAAACAAACAAACAAACAAA=0.00000, CAAACAAACAAACAAACAAACAAA=0.00000, CAAACAAACAAACAAACAAACAAACAAA=0.00000, CAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.00000, CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.00000, CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.00000	1.0	N/A
European	Sub	8602	CAAACAAACAAACAAACAAACAAACAAACAAA=1.0000	CAAACAAACAAACAAACAAA=0.0000, CAAACAAACAAACAAACAAACAAA=0.0000, CAAACAAACAAACAAACAAACAAACAAA=0.0000, CAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.0000, CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.0000, CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.0000	1.0	N/A
African	Sub	1988	CAAACAAACAAACAAACAAACAAACAAACAAA=1.0000	CAAACAAACAAACAAACAAA=0.0000, CAAACAAACAAACAAACAAACAAA=0.0000, CAAACAAACAAACAAACAAACAAACAAA=0.0000, CAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.0000, CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.0000, CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.0000	1.0	N/A
African Others	Sub	82	CAAACAAACAAACAAACAAACAAACAAACAAA=1.00	CAAACAAACAAACAAACAAA=0.00, CAAACAAACAAACAAACAAACAAA=0.00, CAAACAAACAAACAAACAAACAAACAAA=0.00, CAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.00, CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.00, CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.00	1.0	N/A
African American	Sub	1906	CAAACAAACAAACAAACAAACAAACAAACAAA=1.0000	CAAACAAACAAACAAACAAA=0.0000, CAAACAAACAAACAAACAAACAAA=0.0000, CAAACAAACAAACAAACAAACAAACAAA=0.0000, CAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.0000, CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.0000, CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.0000	1.0	N/A
Asian	Sub	106	CAAACAAACAAACAAACAAACAAACAAACAAA=1.000	CAAACAAACAAACAAACAAA=0.000, CAAACAAACAAACAAACAAACAAA=0.000, CAAACAAACAAACAAACAAACAAACAAA=0.000, CAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.000, CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.000, CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.000	1.0	N/A
East Asian	Sub	84	CAAACAAACAAACAAACAAACAAACAAACAAA=1.00	CAAACAAACAAACAAACAAA=0.00, CAAACAAACAAACAAACAAACAAA=0.00, CAAACAAACAAACAAACAAACAAACAAA=0.00, CAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.00, CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.00, CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.00	1.0	N/A
Other Asian	Sub	22	CAAACAAACAAACAAACAAACAAACAAACAAA=1.00	CAAACAAACAAACAAACAAA=0.00, CAAACAAACAAACAAACAAACAAA=0.00, CAAACAAACAAACAAACAAACAAACAAA=0.00, CAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.00, CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.00, CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.00	1.0	N/A
Latin American 1	Sub	122	CAAACAAACAAACAAACAAACAAACAAACAAA=1.000	CAAACAAACAAACAAACAAA=0.000, CAAACAAACAAACAAACAAACAAA=0.000, CAAACAAACAAACAAACAAACAAACAAA=0.000, CAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.000, CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.000, CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.000	1.0	N/A
Latin American 2	Sub	562	CAAACAAACAAACAAACAAACAAACAAACAAA=1.000	CAAACAAACAAACAAACAAA=0.000, CAAACAAACAAACAAACAAACAAA=0.000, CAAACAAACAAACAAACAAACAAACAAA=0.000, CAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.000, CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.000, CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.000	1.0	N/A
South Asian	Sub	94	CAAACAAACAAACAAACAAACAAACAAACAAA=1.00	CAAACAAACAAACAAACAAA=0.00, CAAACAAACAAACAAACAAACAAA=0.00, CAAACAAACAAACAAACAAACAAACAAA=0.00, CAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.00, CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.00, CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.00	1.0	N/A
Other	Sub	408	CAAACAAACAAACAAACAAACAAACAAACAAA=1.000	CAAACAAACAAACAAACAAA=0.000, CAAACAAACAAACAAACAAACAAA=0.000, CAAACAAACAAACAAACAAACAAACAAA=0.000, CAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.000, CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.000, CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA=0.000	1.0	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
Allele Frequency Aggregator	Total	Global	11882	(CAAA)₈=1.00000	del(CAAA)₃=0.00000, del(CAAA)₂=0.00000, delCAAA=0.00000, dupCAAA=0.00000, dup(CAAA)₂=0.00000, dup(CAAA)₃=0.00000
Allele Frequency Aggregator	European	Sub	8602	(CAAA)₈=1.0000	del(CAAA)₃=0.0000, del(CAAA)₂=0.0000, delCAAA=0.0000, dupCAAA=0.0000, dup(CAAA)₂=0.0000, dup(CAAA)₃=0.0000
Allele Frequency Aggregator	African	Sub	1988	(CAAA)₈=1.0000	del(CAAA)₃=0.0000, del(CAAA)₂=0.0000, delCAAA=0.0000, dupCAAA=0.0000, dup(CAAA)₂=0.0000, dup(CAAA)₃=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	562	(CAAA)₈=1.000	del(CAAA)₃=0.000, del(CAAA)₂=0.000, delCAAA=0.000, dupCAAA=0.000, dup(CAAA)₂=0.000, dup(CAAA)₃=0.000
Allele Frequency Aggregator	Other	Sub	408	(CAAA)₈=1.000	del(CAAA)₃=0.000, del(CAAA)₂=0.000, delCAAA=0.000, dupCAAA=0.000, dup(CAAA)₂=0.000, dup(CAAA)₃=0.000
Allele Frequency Aggregator	Latin American 1	Sub	122	(CAAA)₈=1.000	del(CAAA)₃=0.000, del(CAAA)₂=0.000, delCAAA=0.000, dupCAAA=0.000, dup(CAAA)₂=0.000, dup(CAAA)₃=0.000
Allele Frequency Aggregator	Asian	Sub	106	(CAAA)₈=1.000	del(CAAA)₃=0.000, del(CAAA)₂=0.000, delCAAA=0.000, dupCAAA=0.000, dup(CAAA)₂=0.000, dup(CAAA)₃=0.000
Allele Frequency Aggregator	South Asian	Sub	94	(CAAA)₈=1.00	del(CAAA)₃=0.00, del(CAAA)₂=0.00, delCAAA=0.00, dupCAAA=0.00, dup(CAAA)₂=0.00, dup(CAAA)₃=0.00
1000Genomes	Global	Study-wide	5008	(CAAA)₈=0.9593	delCAAA=0.0407
1000Genomes	African	Sub	1322	(CAAA)₈=0.8646	delCAAA=0.1354
1000Genomes	East Asian	Sub	1008	(CAAA)₈=0.9960	delCAAA=0.0040
1000Genomes	Europe	Sub	1006	(CAAA)₈=0.9950	delCAAA=0.0050
1000Genomes	South Asian	Sub	978	(CAAA)₈=0.996	delCAAA=0.004
1000Genomes	American	Sub	694	(CAAA)₈=0.983	delCAAA=0.017
A Vietnamese Genetic Variation Database	Global	Study-wide	216	(CAAA)₈=0.995	delCAAA=0.005
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupCAAA=0.10

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.34419074CAAA[5]
GRCh38.p14 chr 9	NC_000009.12:g.34419074CAAA[6]
GRCh38.p14 chr 9	NC_000009.12:g.34419074CAAA[7]
GRCh38.p14 chr 9	NC_000009.12:g.34419074CAAA[9]
GRCh38.p14 chr 9	NC_000009.12:g.34419074CAAA[10]
GRCh38.p14 chr 9	NC_000009.12:g.34419074CAAA[11]
GRCh38.p14 chr 9	NC_000009.12:g.34419074CAAA[12]
GRCh37.p13 chr 9	NC_000009.11:g.34419072CAAA[5]
GRCh37.p13 chr 9	NC_000009.11:g.34419072CAAA[6]
GRCh37.p13 chr 9	NC_000009.11:g.34419072CAAA[7]
GRCh37.p13 chr 9	NC_000009.11:g.34419072CAAA[9]
GRCh37.p13 chr 9	NC_000009.11:g.34419072CAAA[10]
GRCh37.p13 chr 9	NC_000009.11:g.34419072CAAA[11]
GRCh37.p13 chr 9	NC_000009.11:g.34419072CAAA[12]
FAM219A RefSeqGene	NG_027971.1:g.44466TTTG[5]
FAM219A RefSeqGene	NG_027971.1:g.44466TTTG[6]
FAM219A RefSeqGene	NG_027971.1:g.44466TTTG[7]
FAM219A RefSeqGene	NG_027971.1:g.44466TTTG[9]
FAM219A RefSeqGene	NG_027971.1:g.44466TTTG[10]
FAM219A RefSeqGene	NG_027971.1:g.44466TTTG[11]
FAM219A RefSeqGene	NG_027971.1:g.44466TTTG[12]

Gene: FAM219A, family with sequence similarity 219 member A (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
FAM219A transcript variant 1	NM_001184940.2:c.61-13141… NM_001184940.2:c.61-13141TTTG[5]	N/A	Intron Variant
FAM219A transcript variant 2	NM_001184941.2:c.61-13141… NM_001184941.2:c.61-13141TTTG[5]	N/A	Intron Variant
FAM219A transcript variant 3	NM_001184942.2:c.28-13141… NM_001184942.2:c.28-13141TTTG[5]	N/A	Intron Variant
FAM219A transcript variant 5	NM_001184943.2:c.61-13141… NM_001184943.2:c.61-13141TTTG[5]	N/A	Intron Variant
FAM219A transcript variant 7	NM_001184945.2:c.28-13141… NM_001184945.2:c.28-13141TTTG[5]	N/A	Intron Variant
FAM219A transcript variant 4	NM_147202.2:c.61-13141TTT… NM_147202.2:c.61-13141TTTG[5]	N/A	Intron Variant

Gene: LOC124902145, uncharacterized LOC124902145 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC124902145 transcript	XR_007061465.1:n.	N/A	Intron 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	(CAAA)₈=	del(CAAA)₃	del(CAAA)₂	delCAAA	dupCAAA	dup(CAAA)₂	dup(CAAA)₃	dup(CAAA)₄
GRCh38.p14 chr 9	NC_000009.12:g.34419074_34419105=	NC_000009.12:g.34419074CAAA[5]	NC_000009.12:g.34419074CAAA[6]	NC_000009.12:g.34419074CAAA[7]	NC_000009.12:g.34419074CAAA[9]	NC_000009.12:g.34419074CAAA[10]	NC_000009.12:g.34419074CAAA[11]	NC_000009.12:g.34419074CAAA[12]
GRCh37.p13 chr 9	NC_000009.11:g.34419072_34419103=	NC_000009.11:g.34419072CAAA[5]	NC_000009.11:g.34419072CAAA[6]	NC_000009.11:g.34419072CAAA[7]	NC_000009.11:g.34419072CAAA[9]	NC_000009.11:g.34419072CAAA[10]	NC_000009.11:g.34419072CAAA[11]	NC_000009.11:g.34419072CAAA[12]
FAM219A RefSeqGene	NG_027971.1:g.44466_44497=	NG_027971.1:g.44466TTTG[5]	NG_027971.1:g.44466TTTG[6]	NG_027971.1:g.44466TTTG[7]	NG_027971.1:g.44466TTTG[9]	NG_027971.1:g.44466TTTG[10]	NG_027971.1:g.44466TTTG[11]	NG_027971.1:g.44466TTTG[12]
FAM219A transcript variant 1	NM_001184940.1:c.61-13110=	NM_001184940.1:c.61-13141TTTG[5]	NM_001184940.1:c.61-13141TTTG[6]	NM_001184940.1:c.61-13141TTTG[7]	NM_001184940.1:c.61-13141TTTG[9]	NM_001184940.1:c.61-13141TTTG[10]	NM_001184940.1:c.61-13141TTTG[11]	NM_001184940.1:c.61-13141TTTG[12]
FAM219A transcript variant 1	NM_001184940.2:c.61-13110=	NM_001184940.2:c.61-13141TTTG[5]	NM_001184940.2:c.61-13141TTTG[6]	NM_001184940.2:c.61-13141TTTG[7]	NM_001184940.2:c.61-13141TTTG[9]	NM_001184940.2:c.61-13141TTTG[10]	NM_001184940.2:c.61-13141TTTG[11]	NM_001184940.2:c.61-13141TTTG[12]
FAM219A transcript variant 2	NM_001184941.1:c.61-13110=	NM_001184941.1:c.61-13141TTTG[5]	NM_001184941.1:c.61-13141TTTG[6]	NM_001184941.1:c.61-13141TTTG[7]	NM_001184941.1:c.61-13141TTTG[9]	NM_001184941.1:c.61-13141TTTG[10]	NM_001184941.1:c.61-13141TTTG[11]	NM_001184941.1:c.61-13141TTTG[12]
FAM219A transcript variant 2	NM_001184941.2:c.61-13110=	NM_001184941.2:c.61-13141TTTG[5]	NM_001184941.2:c.61-13141TTTG[6]	NM_001184941.2:c.61-13141TTTG[7]	NM_001184941.2:c.61-13141TTTG[9]	NM_001184941.2:c.61-13141TTTG[10]	NM_001184941.2:c.61-13141TTTG[11]	NM_001184941.2:c.61-13141TTTG[12]
FAM219A transcript variant 3	NM_001184942.1:c.28-13110=	NM_001184942.1:c.28-13141TTTG[5]	NM_001184942.1:c.28-13141TTTG[6]	NM_001184942.1:c.28-13141TTTG[7]	NM_001184942.1:c.28-13141TTTG[9]	NM_001184942.1:c.28-13141TTTG[10]	NM_001184942.1:c.28-13141TTTG[11]	NM_001184942.1:c.28-13141TTTG[12]
FAM219A transcript variant 3	NM_001184942.2:c.28-13110=	NM_001184942.2:c.28-13141TTTG[5]	NM_001184942.2:c.28-13141TTTG[6]	NM_001184942.2:c.28-13141TTTG[7]	NM_001184942.2:c.28-13141TTTG[9]	NM_001184942.2:c.28-13141TTTG[10]	NM_001184942.2:c.28-13141TTTG[11]	NM_001184942.2:c.28-13141TTTG[12]
FAM219A transcript variant 5	NM_001184943.1:c.61-13110=	NM_001184943.1:c.61-13141TTTG[5]	NM_001184943.1:c.61-13141TTTG[6]	NM_001184943.1:c.61-13141TTTG[7]	NM_001184943.1:c.61-13141TTTG[9]	NM_001184943.1:c.61-13141TTTG[10]	NM_001184943.1:c.61-13141TTTG[11]	NM_001184943.1:c.61-13141TTTG[12]
FAM219A transcript variant 5	NM_001184943.2:c.61-13110=	NM_001184943.2:c.61-13141TTTG[5]	NM_001184943.2:c.61-13141TTTG[6]	NM_001184943.2:c.61-13141TTTG[7]	NM_001184943.2:c.61-13141TTTG[9]	NM_001184943.2:c.61-13141TTTG[10]	NM_001184943.2:c.61-13141TTTG[11]	NM_001184943.2:c.61-13141TTTG[12]
FAM219A transcript variant 7	NM_001184945.1:c.28-13110=	NM_001184945.1:c.28-13141TTTG[5]	NM_001184945.1:c.28-13141TTTG[6]	NM_001184945.1:c.28-13141TTTG[7]	NM_001184945.1:c.28-13141TTTG[9]	NM_001184945.1:c.28-13141TTTG[10]	NM_001184945.1:c.28-13141TTTG[11]	NM_001184945.1:c.28-13141TTTG[12]
FAM219A transcript variant 7	NM_001184945.2:c.28-13110=	NM_001184945.2:c.28-13141TTTG[5]	NM_001184945.2:c.28-13141TTTG[6]	NM_001184945.2:c.28-13141TTTG[7]	NM_001184945.2:c.28-13141TTTG[9]	NM_001184945.2:c.28-13141TTTG[10]	NM_001184945.2:c.28-13141TTTG[11]	NM_001184945.2:c.28-13141TTTG[12]
FAM219A transcript variant 4	NM_147202.1:c.61-13110=	NM_147202.1:c.61-13141TTTG[5]	NM_147202.1:c.61-13141TTTG[6]	NM_147202.1:c.61-13141TTTG[7]	NM_147202.1:c.61-13141TTTG[9]	NM_147202.1:c.61-13141TTTG[10]	NM_147202.1:c.61-13141TTTG[11]	NM_147202.1:c.61-13141TTTG[12]
FAM219A transcript variant 4	NM_147202.2:c.61-13110=	NM_147202.2:c.61-13141TTTG[5]	NM_147202.2:c.61-13141TTTG[6]	NM_147202.2:c.61-13141TTTG[7]	NM_147202.2:c.61-13141TTTG[9]	NM_147202.2:c.61-13141TTTG[10]	NM_147202.2:c.61-13141TTTG[11]	NM_147202.2:c.61-13141TTTG[12]
FAM219A transcript variant X1	XM_005251400.1:c.28-13110=	XM_005251400.1:c.28-13141TTTG[5]	XM_005251400.1:c.28-13141TTTG[6]	XM_005251400.1:c.28-13141TTTG[7]	XM_005251400.1:c.28-13141TTTG[9]	XM_005251400.1:c.28-13141TTTG[10]	XM_005251400.1:c.28-13141TTTG[11]	XM_005251400.1:c.28-13141TTTG[12]
FAM219A transcript variant X2	XM_005251401.1:c.28-13110=	XM_005251401.1:c.28-13141TTTG[5]	XM_005251401.1:c.28-13141TTTG[6]	XM_005251401.1:c.28-13141TTTG[7]	XM_005251401.1:c.28-13141TTTG[9]	XM_005251401.1:c.28-13141TTTG[10]	XM_005251401.1:c.28-13141TTTG[11]	XM_005251401.1:c.28-13141TTTG[12]

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#.

63 SubSNP, 32 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss43343806	Mar 13, 2006 (126)
2	HUMANGENOME_JCVI	ss97761050	Feb 05, 2009 (130)
3	1000GENOMES	ss327213066	May 09, 2011 (134)
4	1000GENOMES	ss327570524	Jan 10, 2018 (151)
5	LUNTER	ss551931677	Apr 25, 2013 (138)
6	LUNTER	ss552163170	Apr 25, 2013 (138)
7	LUNTER	ss553374958	Apr 25, 2013 (138)
8	SSMP	ss663920223	Apr 01, 2015 (144)
9	1000GENOMES	ss1368221367	Aug 21, 2014 (142)
10	EVA_GENOME_DK	ss1577366756	Apr 01, 2015 (144)
11	EVA_UK10K_ALSPAC	ss1706390540	Apr 01, 2015 (144)
12	EVA_UK10K_TWINSUK	ss1706390782	Apr 01, 2015 (144)
13	EVA_UK10K_TWINSUK	ss1710420979	Apr 01, 2015 (144)
14	EVA_UK10K_ALSPAC	ss1710421046	Apr 01, 2015 (144)
15	HAMMER_LAB	ss1805968553	Sep 08, 2015 (146)
16	SWEGEN	ss3004698087	Nov 08, 2017 (151)
17	MCHAISSO	ss3066246003	Jan 10, 2018 (151)
18	URBANLAB	ss3649116768	Oct 12, 2018 (152)
19	EVA_DECODE	ss3723853697	Jul 13, 2019 (153)
20	EVA_DECODE	ss3723853698	Jul 13, 2019 (153)
21	EVA_DECODE	ss3723853699	Jul 13, 2019 (153)
22	EVA_DECODE	ss3723853700	Jul 13, 2019 (153)
23	ACPOP	ss3736482329	Jul 13, 2019 (153)
24	ACPOP	ss3736482330	Jul 13, 2019 (153)
25	PACBIO	ss3786400035	Jul 13, 2019 (153)
26	PACBIO	ss3791619227	Jul 13, 2019 (153)
27	PACBIO	ss3796500939	Jul 13, 2019 (153)
28	KHV_HUMAN_GENOMES	ss3812315286	Jul 13, 2019 (153)
29	EVA	ss3831639443	Apr 26, 2020 (154)
30	EVA	ss3839337634	Apr 26, 2020 (154)
31	EVA	ss3844800903	Apr 26, 2020 (154)
32	KOGIC	ss3965661918	Apr 26, 2020 (154)
33	KOGIC	ss3965661919	Apr 26, 2020 (154)
34	GNOMAD	ss4200912526	Apr 26, 2021 (155)
35	GNOMAD	ss4200912527	Apr 26, 2021 (155)
36	GNOMAD	ss4200912528	Apr 26, 2021 (155)
37	GNOMAD	ss4200912529	Apr 26, 2021 (155)
38	GNOMAD	ss4200912530	Apr 26, 2021 (155)
39	GNOMAD	ss4200912531	Apr 26, 2021 (155)
40	TOPMED	ss4819567963	Apr 26, 2021 (155)
41	TOPMED	ss4819567964	Apr 26, 2021 (155)
42	TOPMED	ss4819567965	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5192953587	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5192953588	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5192953589	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5192953590	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5192953591	Apr 26, 2021 (155)
48	1000G_HIGH_COVERAGE	ss5280475880	Oct 16, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5280475881	Oct 16, 2022 (156)
50	1000G_HIGH_COVERAGE	ss5280475882	Oct 16, 2022 (156)
51	1000G_HIGH_COVERAGE	ss5280475883	Oct 16, 2022 (156)
52	HUGCELL_USP	ss5476682678	Oct 16, 2022 (156)
53	HUGCELL_USP	ss5476682679	Oct 16, 2022 (156)
54	HUGCELL_USP	ss5476682680	Oct 16, 2022 (156)
55	TOMMO_GENOMICS	ss5736248959	Oct 16, 2022 (156)
56	TOMMO_GENOMICS	ss5736248960	Oct 16, 2022 (156)
57	TOMMO_GENOMICS	ss5736248961	Oct 16, 2022 (156)
58	TOMMO_GENOMICS	ss5736248962	Oct 16, 2022 (156)
59	TOMMO_GENOMICS	ss5736248963	Oct 16, 2022 (156)
60	TOMMO_GENOMICS	ss5736248964	Oct 16, 2022 (156)
61	EVA	ss5829114411	Oct 16, 2022 (156)
62	EVA	ss5829114412	Oct 16, 2022 (156)
63	EVA	ss5829114413	Oct 16, 2022 (156)
64	1000Genomes	NC_000009.11 - 34419072	Oct 12, 2018 (152)
65	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 25555013 (NC_000009.11:34419071::CAAA 275/3854) Row 25555014 (NC_000009.11:34419071:CAAA: 71/3854)	-	Oct 12, 2018 (152)
66	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 25555013 (NC_000009.11:34419071::CAAA 275/3854) Row 25555014 (NC_000009.11:34419071:CAAA: 71/3854)	-	Oct 12, 2018 (152)
67	The Danish reference pan genome	NC_000009.11 - 34419072	Apr 26, 2020 (154)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 323789486 (NC_000009.12:34419073::CAAA 8994/139678) Row 323789487 (NC_000009.12:34419073::CAAACAAA 134/139700) Row 323789488 (NC_000009.12:34419073::CAAACAAACAAA 6/139700)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 323789486 (NC_000009.12:34419073::CAAA 8994/139678) Row 323789487 (NC_000009.12:34419073::CAAACAAA 134/139700) Row 323789488 (NC_000009.12:34419073::CAAACAAACAAA 6/139700)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 323789486 (NC_000009.12:34419073::CAAA 8994/139678) Row 323789487 (NC_000009.12:34419073::CAAACAAA 134/139700) Row 323789488 (NC_000009.12:34419073::CAAACAAACAAA 6/139700)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 323789486 (NC_000009.12:34419073::CAAA 8994/139678) Row 323789487 (NC_000009.12:34419073::CAAACAAA 134/139700) Row 323789488 (NC_000009.12:34419073::CAAACAAACAAA 6/139700)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 323789486 (NC_000009.12:34419073::CAAA 8994/139678) Row 323789487 (NC_000009.12:34419073::CAAACAAA 134/139700) Row 323789488 (NC_000009.12:34419073::CAAACAAACAAA 6/139700)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 323789486 (NC_000009.12:34419073::CAAA 8994/139678) Row 323789487 (NC_000009.12:34419073::CAAACAAA 134/139700) Row 323789488 (NC_000009.12:34419073::CAAACAAACAAA 6/139700)...	-	Apr 26, 2021 (155)
74	Korean Genome Project Submission ignored due to conflicting rows: Row 22039919 (NC_000009.12:34419073:CAAA: 21/1832) Row 22039920 (NC_000009.12:34419077::CAAA 29/1832)	-	Apr 26, 2020 (154)
75	Korean Genome Project Submission ignored due to conflicting rows: Row 22039919 (NC_000009.12:34419073:CAAA: 21/1832) Row 22039920 (NC_000009.12:34419077::CAAA 29/1832)	-	Apr 26, 2020 (154)
76	Northern Sweden Submission ignored due to conflicting rows: Row 9767194 (NC_000009.11:34419071::CAAA 39/600) Row 9767195 (NC_000009.11:34419071::CAAACAAA 1/600)	-	Jul 13, 2019 (153)
77	Northern Sweden Submission ignored due to conflicting rows: Row 9767194 (NC_000009.11:34419071::CAAA 39/600) Row 9767195 (NC_000009.11:34419071::CAAACAAA 1/600)	-	Jul 13, 2019 (153)
78	8.3KJPN Submission ignored due to conflicting rows: Row 50922894 (NC_000009.11:34419071::CAAA 396/16760) Row 50922895 (NC_000009.11:34419071:CAAA: 149/16760) Row 50922896 (NC_000009.11:34419071:CAAACAAACAAA: 3/16760)...	-	Apr 26, 2021 (155)
79	8.3KJPN Submission ignored due to conflicting rows: Row 50922894 (NC_000009.11:34419071::CAAA 396/16760) Row 50922895 (NC_000009.11:34419071:CAAA: 149/16760) Row 50922896 (NC_000009.11:34419071:CAAACAAACAAA: 3/16760)...	-	Apr 26, 2021 (155)
80	8.3KJPN Submission ignored due to conflicting rows: Row 50922894 (NC_000009.11:34419071::CAAA 396/16760) Row 50922895 (NC_000009.11:34419071:CAAA: 149/16760) Row 50922896 (NC_000009.11:34419071:CAAACAAACAAA: 3/16760)...	-	Apr 26, 2021 (155)
81	8.3KJPN Submission ignored due to conflicting rows: Row 50922894 (NC_000009.11:34419071::CAAA 396/16760) Row 50922895 (NC_000009.11:34419071:CAAA: 149/16760) Row 50922896 (NC_000009.11:34419071:CAAACAAACAAA: 3/16760)...	-	Apr 26, 2021 (155)
82	8.3KJPN Submission ignored due to conflicting rows: Row 50922894 (NC_000009.11:34419071::CAAA 396/16760) Row 50922895 (NC_000009.11:34419071:CAAA: 149/16760) Row 50922896 (NC_000009.11:34419071:CAAACAAACAAA: 3/16760)...	-	Apr 26, 2021 (155)
83	14KJPN Submission ignored due to conflicting rows: Row 70086063 (NC_000009.12:34419073:CAAA: 234/28258) Row 70086064 (NC_000009.12:34419073::CAAA 669/28258) Row 70086065 (NC_000009.12:34419073:CAAACAAACAAA: 3/28258)...	-	Oct 16, 2022 (156)
84	14KJPN Submission ignored due to conflicting rows: Row 70086063 (NC_000009.12:34419073:CAAA: 234/28258) Row 70086064 (NC_000009.12:34419073::CAAA 669/28258) Row 70086065 (NC_000009.12:34419073:CAAACAAACAAA: 3/28258)...	-	Oct 16, 2022 (156)
85	14KJPN Submission ignored due to conflicting rows: Row 70086063 (NC_000009.12:34419073:CAAA: 234/28258) Row 70086064 (NC_000009.12:34419073::CAAA 669/28258) Row 70086065 (NC_000009.12:34419073:CAAACAAACAAA: 3/28258)...	-	Oct 16, 2022 (156)
86	14KJPN Submission ignored due to conflicting rows: Row 70086063 (NC_000009.12:34419073:CAAA: 234/28258) Row 70086064 (NC_000009.12:34419073::CAAA 669/28258) Row 70086065 (NC_000009.12:34419073:CAAACAAACAAA: 3/28258)...	-	Oct 16, 2022 (156)
87	14KJPN Submission ignored due to conflicting rows: Row 70086063 (NC_000009.12:34419073:CAAA: 234/28258) Row 70086064 (NC_000009.12:34419073::CAAA 669/28258) Row 70086065 (NC_000009.12:34419073:CAAACAAACAAA: 3/28258)...	-	Oct 16, 2022 (156)
88	14KJPN Submission ignored due to conflicting rows: Row 70086063 (NC_000009.12:34419073:CAAA: 234/28258) Row 70086064 (NC_000009.12:34419073::CAAA 669/28258) Row 70086065 (NC_000009.12:34419073:CAAACAAACAAA: 3/28258)...	-	Oct 16, 2022 (156)
89	TopMed Submission ignored due to conflicting rows: Row 656945524 (NC_000009.12:34419073::CAAA 16610/264690) Row 656945525 (NC_000009.12:34419073:CAAA: 10812/264690) Row 656945526 (NC_000009.12:34419073:CAAACAAACAAA: 14/264690)	-	Apr 26, 2021 (155)
90	TopMed Submission ignored due to conflicting rows: Row 656945524 (NC_000009.12:34419073::CAAA 16610/264690) Row 656945525 (NC_000009.12:34419073:CAAA: 10812/264690) Row 656945526 (NC_000009.12:34419073:CAAACAAACAAA: 14/264690)	-	Apr 26, 2021 (155)
91	TopMed Submission ignored due to conflicting rows: Row 656945524 (NC_000009.12:34419073::CAAA 16610/264690) Row 656945525 (NC_000009.12:34419073:CAAA: 10812/264690) Row 656945526 (NC_000009.12:34419073:CAAACAAACAAA: 14/264690)	-	Apr 26, 2021 (155)
92	UK 10K study - Twins Submission ignored due to conflicting rows: Row 25555013 (NC_000009.11:34419071::CAAA 224/3708) Row 25555014 (NC_000009.11:34419071:CAAA: 54/3708)	-	Oct 12, 2018 (152)
93	UK 10K study - Twins Submission ignored due to conflicting rows: Row 25555013 (NC_000009.11:34419071::CAAA 224/3708) Row 25555014 (NC_000009.11:34419071:CAAA: 54/3708)	-	Oct 12, 2018 (152)
94	A Vietnamese Genetic Variation Database	NC_000009.11 - 34419072	Jul 13, 2019 (153)
95	ALFA	NC_000009.12 - 34419074	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5192953589	NC_000009.11:34419071:CAAACAAACAAA:	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAA	(self)
ss4200912531, ss4819567965, ss5736248961	NC_000009.12:34419073:CAAACAAACAAA:	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAA	(self)
2124500425	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAA	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAA	(self)
ss5192953590	NC_000009.11:34419071:CAAACAAA:	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAACAAA	(self)
ss3723853700, ss4200912530, ss5280475882, ss5736248962	NC_000009.12:34419073:CAAACAAA:	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAACAAA	(self)
2124500425	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAACAAA	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAACAAA	(self)
ss327570524, ss552163170	NC_000009.10:34409071:CAAA:	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAACAAACAAA	(self)
45943501, 5680790, ss663920223, ss1368221367, ss1706390540, ss1706390782, ss1805968553, ss3004698087, ss5192953588, ss5829114413	NC_000009.11:34419071:CAAA:	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAACAAACAAA	(self)
ss3812315286, ss3965661918, ss4200912529, ss4819567964, ss5280475881, ss5476682679, ss5736248959	NC_000009.12:34419073:CAAA:	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAACAAACAAA	(self)
2124500425	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAACAAACAAA	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAACAAACAAA	(self)
ss3723853699	NC_000009.12:34419077:CAAA:	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAACAAACAAA	(self)
ss327213066, ss551931677, ss553374958	NC_000009.10:34409071::CAAA	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAACAAACAAACAAACAAA	(self)
1273515, ss1577366756, ss3736482329, ss3786400035, ss3791619227, ss3796500939, ss3831639443, ss3839337634, ss5192953587, ss5829114411	NC_000009.11:34419071::CAAA	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAACAAACAAACAAACAAA	(self)
ss1710420979, ss1710421046	NC_000009.11:34419075::CAAA	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAACAAACAAACAAACAAA	(self)
ss3066246003, ss3844800903, ss4200912526, ss4819567963, ss5280475880, ss5476682678, ss5736248960	NC_000009.12:34419073::CAAA	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAACAAACAAACAAACAAA	(self)
2124500425	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAACAAACAAACAAACAAA	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAACAAACAAACAAACAAA	(self)
ss3965661919	NC_000009.12:34419077::CAAA	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAACAAACAAACAAACAAA	(self)
ss3723853698	NC_000009.12:34419081::CAAA	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAACAAACAAACAAACAAA	(self)
ss3649116768	NC_000009.12:34419089::CAAA	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAACAAACAAACAAACAAA	(self)
ss43343806, ss97761050	NT_008413.18:34409103::CAAA	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAACAAACAAACAAACAAA	(self)
ss3736482330, ss5829114412	NC_000009.11:34419071::CAAACAAA	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA	(self)
ss4200912527, ss5280475883, ss5476682680, ss5736248964	NC_000009.12:34419073::CAAACAAA	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA	(self)
2124500425	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA	(self)
ss3723853697	NC_000009.12:34419081::CAAACAAA	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA	(self)
ss4200912528	NC_000009.12:34419073::CAAACAAACAAA	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA	(self)
2124500425	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA	(self)
ss5192953591	NC_000009.11:34419071::CAAACAAACAA… NC_000009.11:34419071::CAAACAAACAAACAAA	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA	(self)
ss5736248963	NC_000009.12:34419073::CAAACAAACAA… NC_000009.12:34419073::CAAACAAACAAACAAA	NC_000009.12:34419073:CAAACAAACAAA… NC_000009.12:34419073:CAAACAAACAAACAAACAAACAAACAAACAAA:CAAACAAACAAACAAACAAACAAACAAACAAACAAACAAACAAACAAA

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

No publications for rs34174911

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
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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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs34174911