Name: rs74178894
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.

rs74178894

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr9:33677010-33677037 (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(CCG)₆ / del(CCG)₅ / del(CCG)₄ …
del(CCG)₆ / del(CCG)₅ / del(CCG)₄ / del(CCG)₃ / del(CCG)₂ / delCCG / dupCCG / dup(CCG)₂ / dup(CCG)₃ / dup(CCG)₄
Variation Type: Indel Insertion and Deletion
Frequency: (GCC)₉G=0.1312 (657/5008, 1000G)
(GCC)₉G=0.1033 (476/4606, ALFA)
del(CCG)₄=0.0010 (4/3854, ALSPAC) (+ 1 more)
(GCC)₉G=0.05 (2/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PTENP1-AS : 2KB Upstream Variant
PTENP1 : Non Coding Transcript 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	4606	GCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.1033	GCCGCCGCCG=0.0000, GCCGCCGCCGCCG=0.0000, GCCGCCGCCGCCGCCG=0.0000, GCCGCCGCCGCCGCCGCCG=0.0000, GCCGCCGCCGCCGCCGCCGCCG=0.0000, GCCGCCGCCGCCGCCGCCGCCGCCG=0.8927, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.0039, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.0000, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.0000, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.0000	0.054243	0.846019	0.099738	32
European	Sub	4462	GCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.0760	GCCGCCGCCG=0.0000, GCCGCCGCCGCCG=0.0000, GCCGCCGCCGCCGCCG=0.0000, GCCGCCGCCGCCGCCGCCG=0.0000, GCCGCCGCCGCCGCCGCCGCCG=0.0000, GCCGCCGCCGCCGCCGCCGCCGCCG=0.9200, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.0040, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.0000, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.0000, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.0000	0.025294	0.872177	0.102529	32
African	Sub	118	GCCGCCGCCGCCGCCGCCGCCGCCGCCG=1.000	GCCGCCGCCG=0.000, GCCGCCGCCGCCG=0.000, GCCGCCGCCGCCGCCG=0.000, GCCGCCGCCGCCGCCGCCG=0.000, GCCGCCGCCGCCGCCGCCGCCG=0.000, GCCGCCGCCGCCGCCGCCGCCGCCG=0.000, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.000, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.000, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.000, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.000	1.0	0.0	0.0	N/A
African Others	Sub	8	GCCGCCGCCGCCGCCGCCGCCGCCGCCG=1.0	GCCGCCGCCG=0.0, GCCGCCGCCGCCG=0.0, GCCGCCGCCGCCGCCG=0.0, GCCGCCGCCGCCGCCGCCG=0.0, GCCGCCGCCGCCGCCGCCGCCG=0.0, GCCGCCGCCGCCGCCGCCGCCGCCG=0.0, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.0, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.0, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.0, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.0	1.0	0.0	0.0	N/A
African American	Sub	110	GCCGCCGCCGCCGCCGCCGCCGCCGCCG=1.000	GCCGCCGCCG=0.000, GCCGCCGCCGCCG=0.000, GCCGCCGCCGCCGCCG=0.000, GCCGCCGCCGCCGCCGCCG=0.000, GCCGCCGCCGCCGCCGCCGCCG=0.000, GCCGCCGCCGCCGCCGCCGCCGCCG=0.000, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.000, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.000, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.000, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.000	1.0	0.0	0.0	N/A
Asian	Sub	0	GCCGCCGCCGCCGCCGCCGCCGCCGCCG=0	GCCGCCGCCG=0, GCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0	0	0	0	N/A
East Asian	Sub	0	GCCGCCGCCGCCGCCGCCGCCGCCGCCG=0	GCCGCCGCCG=0, GCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0	0	0	0	N/A
Other Asian	Sub	0	GCCGCCGCCGCCGCCGCCGCCGCCGCCG=0	GCCGCCGCCG=0, GCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0	0	0	0	N/A
Latin American 1	Sub	0	GCCGCCGCCGCCGCCGCCGCCGCCGCCG=0	GCCGCCGCCG=0, GCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0	0	0	0	N/A
Latin American 2	Sub	4	GCCGCCGCCGCCGCCGCCGCCGCCGCCG=1.0	GCCGCCGCCG=0.0, GCCGCCGCCGCCG=0.0, GCCGCCGCCGCCGCCG=0.0, GCCGCCGCCGCCGCCGCCG=0.0, GCCGCCGCCGCCGCCGCCGCCG=0.0, GCCGCCGCCGCCGCCGCCGCCGCCG=0.0, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.0, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.0, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.0, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.0	1.0	0.0	0.0	N/A
South Asian	Sub	4	GCCGCCGCCGCCGCCGCCGCCGCCGCCG=1.0	GCCGCCGCCG=0.0, GCCGCCGCCGCCG=0.0, GCCGCCGCCGCCGCCG=0.0, GCCGCCGCCGCCGCCGCCG=0.0, GCCGCCGCCGCCGCCGCCGCCG=0.0, GCCGCCGCCGCCGCCGCCGCCGCCG=0.0, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.0, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.0, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.0, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.0	1.0	0.0	0.0	N/A
Other	Sub	18	GCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.61	GCCGCCGCCG=0.00, GCCGCCGCCGCCG=0.00, GCCGCCGCCGCCGCCG=0.00, GCCGCCGCCGCCGCCGCCG=0.00, GCCGCCGCCGCCGCCGCCGCCG=0.00, GCCGCCGCCGCCGCCGCCGCCGCCG=0.39, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.00, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.00, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.00, GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG=0.00	0.555556	0.333333	0.111111	3

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
1000Genomes	Global	Study-wide	5008	(GCC)₉G=0.1312	delCCG=0.8688
1000Genomes	African	Sub	1322	(GCC)₉G=0.2564	delCCG=0.7436
1000Genomes	East Asian	Sub	1008	(GCC)₉G=0.0268	delCCG=0.9732
1000Genomes	Europe	Sub	1006	(GCC)₉G=0.0666	delCCG=0.9334
1000Genomes	South Asian	Sub	978	(GCC)₉G=0.181	delCCG=0.819
1000Genomes	American	Sub	694	(GCC)₉G=0.068	delCCG=0.932
Allele Frequency Aggregator	Total	Global	4606	(GCC)₉G=0.1033	del(CCG)₆=0.0000, del(CCG)₅=0.0000, del(CCG)₄=0.0000, del(CCG)₃=0.0000, del(CCG)₂=0.0000, delCCG=0.8927, dupCCG=0.0039, dup(CCG)₂=0.0000, dup(CCG)₃=0.0000, dup(CCG)₄=0.0000
Allele Frequency Aggregator	European	Sub	4462	(GCC)₉G=0.0760	del(CCG)₆=0.0000, del(CCG)₅=0.0000, del(CCG)₄=0.0000, del(CCG)₃=0.0000, del(CCG)₂=0.0000, delCCG=0.9200, dupCCG=0.0040, dup(CCG)₂=0.0000, dup(CCG)₃=0.0000, dup(CCG)₄=0.0000
Allele Frequency Aggregator	African	Sub	118	(GCC)₉G=1.000	del(CCG)₆=0.000, del(CCG)₅=0.000, del(CCG)₄=0.000, del(CCG)₃=0.000, del(CCG)₂=0.000, delCCG=0.000, dupCCG=0.000, dup(CCG)₂=0.000, dup(CCG)₃=0.000, dup(CCG)₄=0.000
Allele Frequency Aggregator	Other	Sub	18	(GCC)₉G=0.61	del(CCG)₆=0.00, del(CCG)₅=0.00, del(CCG)₄=0.00, del(CCG)₃=0.00, del(CCG)₂=0.00, delCCG=0.39, dupCCG=0.00, dup(CCG)₂=0.00, dup(CCG)₃=0.00, dup(CCG)₄=0.00
Allele Frequency Aggregator	Latin American 2	Sub	4	(GCC)₉G=1.0	del(CCG)₆=0.0, del(CCG)₅=0.0, del(CCG)₄=0.0, del(CCG)₃=0.0, del(CCG)₂=0.0, delCCG=0.0, dupCCG=0.0, dup(CCG)₂=0.0, dup(CCG)₃=0.0, dup(CCG)₄=0.0
Allele Frequency Aggregator	South Asian	Sub	4	(GCC)₉G=1.0	del(CCG)₆=0.0, del(CCG)₅=0.0, del(CCG)₄=0.0, del(CCG)₃=0.0, del(CCG)₂=0.0, delCCG=0.0, dupCCG=0.0, dup(CCG)₂=0.0, dup(CCG)₃=0.0, dup(CCG)₄=0.0
Allele Frequency Aggregator	Latin American 1	Sub	0	(GCC)₉G=0	del(CCG)₆=0, del(CCG)₅=0, del(CCG)₄=0, del(CCG)₃=0, del(CCG)₂=0, delCCG=0, dupCCG=0, dup(CCG)₂=0, dup(CCG)₃=0, dup(CCG)₄=0
Allele Frequency Aggregator	Asian	Sub	0	(GCC)₉G=0	del(CCG)₆=0, del(CCG)₅=0, del(CCG)₄=0, del(CCG)₃=0, del(CCG)₂=0, delCCG=0, dupCCG=0, dup(CCG)₂=0, dup(CCG)₃=0, dup(CCG)₄=0
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(GCC)₉G=0.9990	del(CCG)₄=0.0010
The Danish reference pan genome	Danish	Study-wide	40	(GCC)₉G=0.05	delCCG=0.95

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.33677011CCG[3]
GRCh38.p14 chr 9	NC_000009.12:g.33677011CCG[4]
GRCh38.p14 chr 9	NC_000009.12:g.33677011CCG[5]
GRCh38.p14 chr 9	NC_000009.12:g.33677011CCG[6]
GRCh38.p14 chr 9	NC_000009.12:g.33677011CCG[7]
GRCh38.p14 chr 9	NC_000009.12:g.33677011CCG[8]
GRCh38.p14 chr 9	NC_000009.12:g.33677011CCG[10]
GRCh38.p14 chr 9	NC_000009.12:g.33677011CCG[11]
GRCh38.p14 chr 9	NC_000009.12:g.33677011CCG[12]
GRCh38.p14 chr 9	NC_000009.12:g.33677011CCG[13]
GRCh37.p13 chr 9	NC_000009.11:g.33677009CCG[3]
GRCh37.p13 chr 9	NC_000009.11:g.33677009CCG[4]
GRCh37.p13 chr 9	NC_000009.11:g.33677009CCG[5]
GRCh37.p13 chr 9	NC_000009.11:g.33677009CCG[6]
GRCh37.p13 chr 9	NC_000009.11:g.33677009CCG[7]
GRCh37.p13 chr 9	NC_000009.11:g.33677009CCG[8]
GRCh37.p13 chr 9	NC_000009.11:g.33677009CCG[10]
GRCh37.p13 chr 9	NC_000009.11:g.33677009CCG[11]
GRCh37.p13 chr 9	NC_000009.11:g.33677009CCG[12]
GRCh37.p13 chr 9	NC_000009.11:g.33677009CCG[13]
TRBV/OR9 genomic region	NG_001337.2:g.70551CCG[3]
TRBV/OR9 genomic region	NG_001337.2:g.70551CCG[4]
TRBV/OR9 genomic region	NG_001337.2:g.70551CCG[5]
TRBV/OR9 genomic region	NG_001337.2:g.70551CCG[6]
TRBV/OR9 genomic region	NG_001337.2:g.70551CCG[7]
TRBV/OR9 genomic region	NG_001337.2:g.70551CCG[8]
TRBV/OR9 genomic region	NG_001337.2:g.70551CCG[10]
TRBV/OR9 genomic region	NG_001337.2:g.70551CCG[11]
TRBV/OR9 genomic region	NG_001337.2:g.70551CCG[12]
TRBV/OR9 genomic region	NG_001337.2:g.70551CCG[13]

Gene: PTENP1, phosphatase and tensin homolog pseudogene 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PTENP1 transcript	NR_023917.1:n.385GGC[3]	N/A	Non Coding Transcript Variant
PTENP1 transcript	NR_023917.1:n.385GGC[4]	N/A	Non Coding Transcript Variant
PTENP1 transcript	NR_023917.1:n.385GGC[5]	N/A	Non Coding Transcript Variant
PTENP1 transcript	NR_023917.1:n.385GGC[6]	N/A	Non Coding Transcript Variant
PTENP1 transcript	NR_023917.1:n.385GGC[7]	N/A	Non Coding Transcript Variant
PTENP1 transcript	NR_023917.1:n.385GGC[8]	N/A	Non Coding Transcript Variant
PTENP1 transcript	NR_023917.1:n.385GGC[10]	N/A	Non Coding Transcript Variant
PTENP1 transcript	NR_023917.1:n.385GGC[11]	N/A	Non Coding Transcript Variant
PTENP1 transcript	NR_023917.1:n.385GGC[12]	N/A	Non Coding Transcript Variant
PTENP1 transcript	NR_023917.1:n.385GGC[13]	N/A	Non Coding Transcript Variant

Gene: PTENP1-AS, PTENP1 antisense RNA (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
PTENP1-AS transcript	NR_103745.2:n.	N/A	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	(GCC)₉G=	del(CCG)₆	del(CCG)₅	del(CCG)₄	del(CCG)₃	del(CCG)₂	delCCG	dupCCG	dup(CCG)₂	dup(CCG)₃	dup(CCG)₄
GRCh38.p14 chr 9	NC_000009.12:g.33677010_33677037=	NC_000009.12:g.33677011CCG[3]	NC_000009.12:g.33677011CCG[4]	NC_000009.12:g.33677011CCG[5]	NC_000009.12:g.33677011CCG[6]	NC_000009.12:g.33677011CCG[7]	NC_000009.12:g.33677011CCG[8]	NC_000009.12:g.33677011CCG[10]	NC_000009.12:g.33677011CCG[11]	NC_000009.12:g.33677011CCG[12]	NC_000009.12:g.33677011CCG[13]
GRCh37.p13 chr 9	NC_000009.11:g.33677008_33677035=	NC_000009.11:g.33677009CCG[3]	NC_000009.11:g.33677009CCG[4]	NC_000009.11:g.33677009CCG[5]	NC_000009.11:g.33677009CCG[6]	NC_000009.11:g.33677009CCG[7]	NC_000009.11:g.33677009CCG[8]	NC_000009.11:g.33677009CCG[10]	NC_000009.11:g.33677009CCG[11]	NC_000009.11:g.33677009CCG[12]	NC_000009.11:g.33677009CCG[13]
TRBV/OR9 genomic region	NG_001337.2:g.70550_70577=	NG_001337.2:g.70551CCG[3]	NG_001337.2:g.70551CCG[4]	NG_001337.2:g.70551CCG[5]	NG_001337.2:g.70551CCG[6]	NG_001337.2:g.70551CCG[7]	NG_001337.2:g.70551CCG[8]	NG_001337.2:g.70551CCG[10]	NG_001337.2:g.70551CCG[11]	NG_001337.2:g.70551CCG[12]	NG_001337.2:g.70551CCG[13]
PTENP1 transcript	NR_023917.1:n.384_411=	NR_023917.1:n.385GGC[3]	NR_023917.1:n.385GGC[4]	NR_023917.1:n.385GGC[5]	NR_023917.1:n.385GGC[6]	NR_023917.1:n.385GGC[7]	NR_023917.1:n.385GGC[8]	NR_023917.1:n.385GGC[10]	NR_023917.1:n.385GGC[11]	NR_023917.1:n.385GGC[12]	NR_023917.1:n.385GGC[13]

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#.

65 SubSNP, 25 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95514987	Feb 16, 2009 (130)
2	BCMHGSC_JDW	ss103781726	Dec 01, 2009 (131)
3	LUNTER	ss551931068	Apr 25, 2013 (138)
4	LUNTER	ss553374738	Apr 25, 2013 (138)
5	SSMP	ss663919668	Apr 01, 2015 (144)
6	1000GENOMES	ss1368219492	Aug 21, 2014 (142)
7	EVA_GENOME_DK	ss1577364477	Apr 01, 2015 (144)
8	EVA_UK10K_ALSPAC	ss1706387881	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1706388009	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1710420490	Apr 01, 2015 (144)
11	EVA_UK10K_ALSPAC	ss1710420533	Apr 01, 2015 (144)
12	SWEGEN	ss3004688145	Nov 08, 2017 (151)
13	MCHAISSO	ss3064333128	Nov 08, 2017 (151)
14	MCHAISSO	ss3065223792	Nov 08, 2017 (151)
15	MCHAISSO	ss3066245649	Nov 08, 2017 (151)
16	BEROUKHIMLAB	ss3644279656	Oct 12, 2018 (152)
17	URBANLAB	ss3649115489	Oct 12, 2018 (152)
18	EVA_DECODE	ss3723841920	Jul 13, 2019 (153)
19	EVA_DECODE	ss3723841921	Jul 13, 2019 (153)
20	EVA_DECODE	ss3723841922	Jul 13, 2019 (153)
21	EVA_DECODE	ss3723841923	Jul 13, 2019 (153)
22	EVA_DECODE	ss3723841924	Jul 13, 2019 (153)
23	EVA_DECODE	ss3723841925	Jul 13, 2019 (153)
24	ACPOP	ss3736477589	Jul 13, 2019 (153)
25	ACPOP	ss3736477590	Jul 13, 2019 (153)
26	PACBIO	ss3786398362	Jul 13, 2019 (153)
27	PACBIO	ss3791617837	Jul 13, 2019 (153)
28	PACBIO	ss3796499534	Jul 13, 2019 (153)
29	KHV_HUMAN_GENOMES	ss3812309517	Jul 13, 2019 (153)
30	EVA	ss3831636433	Apr 26, 2020 (154)
31	EVA	ss3839335960	Apr 26, 2020 (154)
32	EVA	ss3844799193	Apr 26, 2020 (154)
33	EVA	ss3986045929	Apr 26, 2021 (155)
34	GNOMAD	ss4200815979	Apr 26, 2021 (155)
35	GNOMAD	ss4200815980	Apr 26, 2021 (155)
36	GNOMAD	ss4200815981	Apr 26, 2021 (155)
37	GNOMAD	ss4200815982	Apr 26, 2021 (155)
38	GNOMAD	ss4200815983	Apr 26, 2021 (155)
39	GNOMAD	ss4200815984	Apr 26, 2021 (155)
40	GNOMAD	ss4200815985	Apr 26, 2021 (155)
41	GNOMAD	ss4200815986	Apr 26, 2021 (155)
42	GNOMAD	ss4200815987	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5192927376	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5192927377	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5192927378	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5192927379	Apr 26, 2021 (155)
47	1000G_HIGH_COVERAGE	ss5280457244	Oct 13, 2022 (156)
48	1000G_HIGH_COVERAGE	ss5280457245	Oct 13, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5280457246	Oct 13, 2022 (156)
50	1000G_HIGH_COVERAGE	ss5280457247	Oct 13, 2022 (156)
51	HUGCELL_USP	ss5476666463	Oct 13, 2022 (156)
52	HUGCELL_USP	ss5476666464	Oct 13, 2022 (156)
53	HUGCELL_USP	ss5476666465	Oct 13, 2022 (156)
54	HUGCELL_USP	ss5476666466	Oct 13, 2022 (156)
55	EVA	ss5509699151	Oct 13, 2022 (156)
56	TOMMO_GENOMICS	ss5736212558	Oct 13, 2022 (156)
57	TOMMO_GENOMICS	ss5736212559	Oct 13, 2022 (156)
58	TOMMO_GENOMICS	ss5736212560	Oct 13, 2022 (156)
59	TOMMO_GENOMICS	ss5736212561	Oct 13, 2022 (156)
60	EVA	ss5829107217	Oct 13, 2022 (156)
61	EVA	ss5829107218	Oct 13, 2022 (156)
62	EVA	ss5829107219	Oct 13, 2022 (156)
63	EVA	ss5856754046	Oct 13, 2022 (156)
64	EVA	ss5916284742	Oct 13, 2022 (156)
65	EVA	ss5980550179	Oct 13, 2022 (156)
66	1000Genomes	NC_000009.11 - 33677008	Oct 12, 2018 (152)
67	The Avon Longitudinal Study of Parents and Children	NC_000009.11 - 33677008	Oct 12, 2018 (152)
68	The Danish reference pan genome	NC_000009.11 - 33677008	Apr 26, 2020 (154)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 323632196 (NC_000009.12:33677009::GCC 345/134940) Row 323632197 (NC_000009.12:33677009::GCCGCC 265/134938) Row 323632198 (NC_000009.12:33677009::GCCGCCGCC 7/134940)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 323632196 (NC_000009.12:33677009::GCC 345/134940) Row 323632197 (NC_000009.12:33677009::GCCGCC 265/134938) Row 323632198 (NC_000009.12:33677009::GCCGCCGCC 7/134940)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 323632196 (NC_000009.12:33677009::GCC 345/134940) Row 323632197 (NC_000009.12:33677009::GCCGCC 265/134938) Row 323632198 (NC_000009.12:33677009::GCCGCCGCC 7/134940)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 323632196 (NC_000009.12:33677009::GCC 345/134940) Row 323632197 (NC_000009.12:33677009::GCCGCC 265/134938) Row 323632198 (NC_000009.12:33677009::GCCGCCGCC 7/134940)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 323632196 (NC_000009.12:33677009::GCC 345/134940) Row 323632197 (NC_000009.12:33677009::GCCGCC 265/134938) Row 323632198 (NC_000009.12:33677009::GCCGCCGCC 7/134940)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 323632196 (NC_000009.12:33677009::GCC 345/134940) Row 323632197 (NC_000009.12:33677009::GCCGCC 265/134938) Row 323632198 (NC_000009.12:33677009::GCCGCCGCC 7/134940)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 323632196 (NC_000009.12:33677009::GCC 345/134940) Row 323632197 (NC_000009.12:33677009::GCCGCC 265/134938) Row 323632198 (NC_000009.12:33677009::GCCGCCGCC 7/134940)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 323632196 (NC_000009.12:33677009::GCC 345/134940) Row 323632197 (NC_000009.12:33677009::GCCGCC 265/134938) Row 323632198 (NC_000009.12:33677009::GCCGCCGCC 7/134940)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 323632196 (NC_000009.12:33677009::GCC 345/134940) Row 323632197 (NC_000009.12:33677009::GCCGCC 265/134938) Row 323632198 (NC_000009.12:33677009::GCCGCCGCC 7/134940)...	-	Apr 26, 2021 (155)
78	Northern Sweden Submission ignored due to conflicting rows: Row 9762454 (NC_000009.11:33677007:GCC: 556/600) Row 9762455 (NC_000009.11:33677007::GCC 2/600)	-	Jul 13, 2019 (153)
79	Northern Sweden Submission ignored due to conflicting rows: Row 9762454 (NC_000009.11:33677007:GCC: 556/600) Row 9762455 (NC_000009.11:33677007::GCC 2/600)	-	Jul 13, 2019 (153)
80	8.3KJPN Submission ignored due to conflicting rows: Row 50896683 (NC_000009.11:33677007:GCC: 15761/16630) Row 50896684 (NC_000009.11:33677007:GCCGCCGCCGCC: 243/16630) Row 50896685 (NC_000009.11:33677007::GCCGCC 1/16630)...	-	Apr 26, 2021 (155)
81	8.3KJPN Submission ignored due to conflicting rows: Row 50896683 (NC_000009.11:33677007:GCC: 15761/16630) Row 50896684 (NC_000009.11:33677007:GCCGCCGCCGCC: 243/16630) Row 50896685 (NC_000009.11:33677007::GCCGCC 1/16630)...	-	Apr 26, 2021 (155)
82	8.3KJPN Submission ignored due to conflicting rows: Row 50896683 (NC_000009.11:33677007:GCC: 15761/16630) Row 50896684 (NC_000009.11:33677007:GCCGCCGCCGCC: 243/16630) Row 50896685 (NC_000009.11:33677007::GCCGCC 1/16630)...	-	Apr 26, 2021 (155)
83	8.3KJPN Submission ignored due to conflicting rows: Row 50896683 (NC_000009.11:33677007:GCC: 15761/16630) Row 50896684 (NC_000009.11:33677007:GCCGCCGCCGCC: 243/16630) Row 50896685 (NC_000009.11:33677007::GCCGCC 1/16630)...	-	Apr 26, 2021 (155)
84	14KJPN Submission ignored due to conflicting rows: Row 70049662 (NC_000009.12:33677009:GCC: 26016/27978) Row 70049663 (NC_000009.12:33677009:GCCGCCGCCGCC: 376/27978) Row 70049664 (NC_000009.12:33677009::GCCGCC 2/27978)...	-	Oct 13, 2022 (156)
85	14KJPN Submission ignored due to conflicting rows: Row 70049662 (NC_000009.12:33677009:GCC: 26016/27978) Row 70049663 (NC_000009.12:33677009:GCCGCCGCCGCC: 376/27978) Row 70049664 (NC_000009.12:33677009::GCCGCC 2/27978)...	-	Oct 13, 2022 (156)
86	14KJPN Submission ignored due to conflicting rows: Row 70049662 (NC_000009.12:33677009:GCC: 26016/27978) Row 70049663 (NC_000009.12:33677009:GCCGCCGCCGCC: 376/27978) Row 70049664 (NC_000009.12:33677009::GCCGCC 2/27978)...	-	Oct 13, 2022 (156)
87	14KJPN Submission ignored due to conflicting rows: Row 70049662 (NC_000009.12:33677009:GCC: 26016/27978) Row 70049663 (NC_000009.12:33677009:GCCGCCGCCGCC: 376/27978) Row 70049664 (NC_000009.12:33677009::GCCGCC 2/27978)...	-	Oct 13, 2022 (156)
88	UK 10K study - Twins Submission ignored due to conflicting rows: Row 25543764 (NC_000009.11:33677016:GCC: 3407/3708) Row 25543765 (NC_000009.11:33677007:GCCGCCGCCGCC: 2/3708)	-	Apr 26, 2020 (154)
89	UK 10K study - Twins	-	Oct 12, 2018 (152)
90	ALFA	NC_000009.12 - 33677010	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
ss4200815987	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCC:	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCG	(self)
4576153061	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCG	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCG	(self)
ss3723841925, ss4200815986	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCC:	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCG	(self)
4576153061	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCG	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCG	(self)
25543765, ss1706387881, ss1706388009, ss3004688145, ss5192927377	NC_000009.11:33677007:GCCGCCGCCGCC:	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCG	(self)
ss4200815985, ss5280457247, ss5476666466, ss5736212559	NC_000009.12:33677009:GCCGCCGCCGCC:	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCG	(self)
4576153061	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCG	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCG	(self)
ss3723841924	NC_000009.12:33677012:GCCGCCGCCGCC:	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCG	(self)
ss5192927379	NC_000009.11:33677007:GCCGCCGCC:	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCG	(self)
ss4200815984, ss5736212561	NC_000009.12:33677009:GCCGCCGCC:	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCG	(self)
4576153061	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCG	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCG	(self)
ss3723841923	NC_000009.12:33677015:GCCGCCGCC:	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCG	(self)
ss5829107219	NC_000009.11:33677007:GCCGCC:	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCGCCG
ss4200815983	NC_000009.12:33677009:GCCGCC:	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCGCCG	(self)
4576153061	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCGCCG	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCGCCG	(self)
ss3723841922	NC_000009.12:33677018:GCCGCC:	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCGCCG	(self)
ss551931068, ss553374738	NC_000009.10:33667007:GCC:	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCGCCGCCG	(self)
45923467, 1272997, ss663919668, ss1368219492, ss1577364477, ss3644279656, ss3736477589, ss3786398362, ss3791617837, ss3796499534, ss3831636433, ss3839335960, ss3986045929, ss5192927376, ss5509699151, ss5829107217, ss5980550179	NC_000009.11:33677007:GCC:	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCGCCGCCG	(self)
ss1710420490, ss1710420533	NC_000009.11:33677016:GCC:	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCGCCGCCG	(self)
ss3064333128, ss3065223792, ss3066245649, ss3812309517, ss3844799193, ss4200815982, ss5280457244, ss5476666463, ss5736212558, ss5856754046, ss5916284742	NC_000009.12:33677009:GCC:	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCGCCGCCG	(self)
4576153061	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCGCCGCCG	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCGCCGCCG	(self)
ss3723841921	NC_000009.12:33677021:GCC:	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCGCCGCCG	(self)
ss3649115489	NC_000009.12:33677033:GCC:	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCGCCGCCG	(self)
ss95514987	NT_008413.18:33667029:CCG:	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCGCCGCCG	(self)
ss103781726	NT_008413.18:33667032:CCG:	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCGCCGCCG	(self)
ss3736477590, ss5829107218	NC_000009.11:33677007::GCC	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG	(self)
ss4200815979, ss5280457245, ss5476666465	NC_000009.12:33677009::GCC	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG	(self)
4576153061	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG	(self)
ss3723841920	NC_000009.12:33677024::GCC	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG	(self)
ss5192927378	NC_000009.11:33677007::GCCGCC	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG	(self)
ss4200815980, ss5280457246, ss5476666464, ss5736212560	NC_000009.12:33677009::GCCGCC	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG	(self)
4576153061	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG	(self)
ss4200815981	NC_000009.12:33677009::GCCGCCGCC	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG	(self)
4576153061	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG	(self)
4576153061	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3587002260	NC_000009.12:33677009::GCCGCCGCCGCC	NC_000009.12:33677009:GCCGCCGCCGCC… NC_000009.12:33677009:GCCGCCGCCGCCGCCGCCGCCGCCGCCG:GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG

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

No publications for rs74178894

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

rs74178894