Name: rs59791059
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.

rs59791059

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:3354460-3354479 (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(A)₉ / del(A)₅ / del(A)₄ / delA…
del(A)₉ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₇
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₉=0.0000 (0/2154, ALFA)
del(A)₅=0.0000 (0/2154, ALFA)
del(A)₄=0.0000 (0/2154, ALFA) (+ 9 more)
delAAA=0.0000 (0/2154, ALFA)
delAA=0.0000 (0/2154, ALFA)
delA=0.0000 (0/2154, ALFA)
dupA=0.0000 (0/2154, ALFA)
dupAA=0.0000 (0/2154, ALFA)
dupAAA=0.0000 (0/2154, ALFA)
dup(A)₄=0.0000 (0/2154, ALFA)
dup(A)₅=0.0000 (0/2154, ALFA)
dupA=0.4 (3/8, KOREAN)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PRDM16 : 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	2154	AAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	1664	AAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	146	AAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	4	AAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
African American	Sub	142	AAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	24	AAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	12	AAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	12	AAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	28	AAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	186	AAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	16	AAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	90	AAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	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	2154	(A)₂₀=1.0000	del(A)₉=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000
Allele Frequency Aggregator	European	Sub	1664	(A)₂₀=1.0000	del(A)₉=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	186	(A)₂₀=1.000	del(A)₉=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	African	Sub	146	(A)₂₀=1.000	del(A)₉=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Other	Sub	90	(A)₂₀=1.00	del(A)₉=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	Latin American 1	Sub	28	(A)₂₀=1.00	del(A)₉=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	Asian	Sub	24	(A)₂₀=1.00	del(A)₉=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	16	(A)₂₀=1.00	del(A)₉=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
KOREAN population from KRGDB	KOREAN	Study-wide	8	- No frequency provided	dupA=0.4

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 1	NC_000001.11:g.3354471_3354479del
GRCh38.p14 chr 1	NC_000001.11:g.3354475_3354479del
GRCh38.p14 chr 1	NC_000001.11:g.3354476_3354479del
GRCh38.p14 chr 1	NC_000001.11:g.3354477_3354479del
GRCh38.p14 chr 1	NC_000001.11:g.3354478_3354479del
GRCh38.p14 chr 1	NC_000001.11:g.3354479del
GRCh38.p14 chr 1	NC_000001.11:g.3354479dup
GRCh38.p14 chr 1	NC_000001.11:g.3354478_3354479dup
GRCh38.p14 chr 1	NC_000001.11:g.3354477_3354479dup
GRCh38.p14 chr 1	NC_000001.11:g.3354476_3354479dup
GRCh38.p14 chr 1	NC_000001.11:g.3354475_3354479dup
GRCh38.p14 chr 1	NC_000001.11:g.3354474_3354479dup
GRCh38.p14 chr 1	NC_000001.11:g.3354473_3354479dup
GRCh37.p13 chr 1	NC_000001.10:g.3271035_3271043del
GRCh37.p13 chr 1	NC_000001.10:g.3271039_3271043del
GRCh37.p13 chr 1	NC_000001.10:g.3271040_3271043del
GRCh37.p13 chr 1	NC_000001.10:g.3271041_3271043del
GRCh37.p13 chr 1	NC_000001.10:g.3271042_3271043del
GRCh37.p13 chr 1	NC_000001.10:g.3271043del
GRCh37.p13 chr 1	NC_000001.10:g.3271043dup
GRCh37.p13 chr 1	NC_000001.10:g.3271042_3271043dup
GRCh37.p13 chr 1	NC_000001.10:g.3271041_3271043dup
GRCh37.p13 chr 1	NC_000001.10:g.3271040_3271043dup
GRCh37.p13 chr 1	NC_000001.10:g.3271039_3271043dup
GRCh37.p13 chr 1	NC_000001.10:g.3271038_3271043dup
GRCh37.p13 chr 1	NC_000001.10:g.3271037_3271043dup
PRDM16 RefSeqGene	NG_029576.2:g.290294_290302del
PRDM16 RefSeqGene	NG_029576.2:g.290298_290302del
PRDM16 RefSeqGene	NG_029576.2:g.290299_290302del
PRDM16 RefSeqGene	NG_029576.2:g.290300_290302del
PRDM16 RefSeqGene	NG_029576.2:g.290301_290302del
PRDM16 RefSeqGene	NG_029576.2:g.290302del
PRDM16 RefSeqGene	NG_029576.2:g.290302dup
PRDM16 RefSeqGene	NG_029576.2:g.290301_290302dup
PRDM16 RefSeqGene	NG_029576.2:g.290300_290302dup
PRDM16 RefSeqGene	NG_029576.2:g.290299_290302dup
PRDM16 RefSeqGene	NG_029576.2:g.290298_290302dup
PRDM16 RefSeqGene	NG_029576.2:g.290297_290302dup
PRDM16 RefSeqGene	NG_029576.2:g.290296_290302dup

Gene: PRDM16, PR/SET domain 16 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PRDM16 transcript variant 1	NM_022114.4:c.439-30681_4… NM_022114.4:c.439-30681_439-30673del	N/A	Intron Variant
PRDM16 transcript variant 2	NM_199454.3:c.439-30681_4… NM_199454.3:c.439-30681_439-30673del	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	(A)₂₀=	del(A)₉	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₇
GRCh38.p14 chr 1	NC_000001.11:g.3354460_3354479=	NC_000001.11:g.3354471_3354479del	NC_000001.11:g.3354475_3354479del	NC_000001.11:g.3354476_3354479del	NC_000001.11:g.3354477_3354479del	NC_000001.11:g.3354478_3354479del	NC_000001.11:g.3354479del	NC_000001.11:g.3354479dup	NC_000001.11:g.3354478_3354479dup	NC_000001.11:g.3354477_3354479dup	NC_000001.11:g.3354476_3354479dup	NC_000001.11:g.3354475_3354479dup	NC_000001.11:g.3354474_3354479dup	NC_000001.11:g.3354473_3354479dup
GRCh37.p13 chr 1	NC_000001.10:g.3271024_3271043=	NC_000001.10:g.3271035_3271043del	NC_000001.10:g.3271039_3271043del	NC_000001.10:g.3271040_3271043del	NC_000001.10:g.3271041_3271043del	NC_000001.10:g.3271042_3271043del	NC_000001.10:g.3271043del	NC_000001.10:g.3271043dup	NC_000001.10:g.3271042_3271043dup	NC_000001.10:g.3271041_3271043dup	NC_000001.10:g.3271040_3271043dup	NC_000001.10:g.3271039_3271043dup	NC_000001.10:g.3271038_3271043dup	NC_000001.10:g.3271037_3271043dup
PRDM16 RefSeqGene	NG_029576.2:g.290283_290302=	NG_029576.2:g.290294_290302del	NG_029576.2:g.290298_290302del	NG_029576.2:g.290299_290302del	NG_029576.2:g.290300_290302del	NG_029576.2:g.290301_290302del	NG_029576.2:g.290302del	NG_029576.2:g.290302dup	NG_029576.2:g.290301_290302dup	NG_029576.2:g.290300_290302dup	NG_029576.2:g.290299_290302dup	NG_029576.2:g.290298_290302dup	NG_029576.2:g.290297_290302dup	NG_029576.2:g.290296_290302dup
PRDM16 transcript variant 1	NM_022114.3:c.439-30692=	NM_022114.3:c.439-30681_439-30673del	NM_022114.3:c.439-30677_439-30673del	NM_022114.3:c.439-30676_439-30673del	NM_022114.3:c.439-30675_439-30673del	NM_022114.3:c.439-30674_439-30673del	NM_022114.3:c.439-30673del	NM_022114.3:c.439-30673dup	NM_022114.3:c.439-30674_439-30673dup	NM_022114.3:c.439-30675_439-30673dup	NM_022114.3:c.439-30676_439-30673dup	NM_022114.3:c.439-30677_439-30673dup	NM_022114.3:c.439-30678_439-30673dup	NM_022114.3:c.439-30679_439-30673dup
PRDM16 transcript variant 1	NM_022114.4:c.439-30692=	NM_022114.4:c.439-30681_439-30673del	NM_022114.4:c.439-30677_439-30673del	NM_022114.4:c.439-30676_439-30673del	NM_022114.4:c.439-30675_439-30673del	NM_022114.4:c.439-30674_439-30673del	NM_022114.4:c.439-30673del	NM_022114.4:c.439-30673dup	NM_022114.4:c.439-30674_439-30673dup	NM_022114.4:c.439-30675_439-30673dup	NM_022114.4:c.439-30676_439-30673dup	NM_022114.4:c.439-30677_439-30673dup	NM_022114.4:c.439-30678_439-30673dup	NM_022114.4:c.439-30679_439-30673dup
PRDM16 transcript variant 2	NM_199454.2:c.439-30692=	NM_199454.2:c.439-30681_439-30673del	NM_199454.2:c.439-30677_439-30673del	NM_199454.2:c.439-30676_439-30673del	NM_199454.2:c.439-30675_439-30673del	NM_199454.2:c.439-30674_439-30673del	NM_199454.2:c.439-30673del	NM_199454.2:c.439-30673dup	NM_199454.2:c.439-30674_439-30673dup	NM_199454.2:c.439-30675_439-30673dup	NM_199454.2:c.439-30676_439-30673dup	NM_199454.2:c.439-30677_439-30673dup	NM_199454.2:c.439-30678_439-30673dup	NM_199454.2:c.439-30679_439-30673dup
PRDM16 transcript variant 2	NM_199454.3:c.439-30692=	NM_199454.3:c.439-30681_439-30673del	NM_199454.3:c.439-30677_439-30673del	NM_199454.3:c.439-30676_439-30673del	NM_199454.3:c.439-30675_439-30673del	NM_199454.3:c.439-30674_439-30673del	NM_199454.3:c.439-30673del	NM_199454.3:c.439-30673dup	NM_199454.3:c.439-30674_439-30673dup	NM_199454.3:c.439-30675_439-30673dup	NM_199454.3:c.439-30676_439-30673dup	NM_199454.3:c.439-30677_439-30673dup	NM_199454.3:c.439-30678_439-30673dup	NM_199454.3:c.439-30679_439-30673dup
PRDM16 transcript variant X1	XM_005244772.1:c.439-30689=	XM_005244772.1:c.439-30678_439-30670del	XM_005244772.1:c.439-30674_439-30670del	XM_005244772.1:c.439-30673_439-30670del	XM_005244772.1:c.439-30672_439-30670del	XM_005244772.1:c.439-30671_439-30670del	XM_005244772.1:c.439-30670del	XM_005244772.1:c.439-30670dup	XM_005244772.1:c.439-30671_439-30670dup	XM_005244772.1:c.439-30672_439-30670dup	XM_005244772.1:c.439-30673_439-30670dup	XM_005244772.1:c.439-30674_439-30670dup	XM_005244772.1:c.439-30675_439-30670dup	XM_005244772.1:c.439-30676_439-30670dup
PRDM16 transcript variant X2	XM_005244773.1:c.439-30689=	XM_005244773.1:c.439-30678_439-30670del	XM_005244773.1:c.439-30674_439-30670del	XM_005244773.1:c.439-30673_439-30670del	XM_005244773.1:c.439-30672_439-30670del	XM_005244773.1:c.439-30671_439-30670del	XM_005244773.1:c.439-30670del	XM_005244773.1:c.439-30670dup	XM_005244773.1:c.439-30671_439-30670dup	XM_005244773.1:c.439-30672_439-30670dup	XM_005244773.1:c.439-30673_439-30670dup	XM_005244773.1:c.439-30674_439-30670dup	XM_005244773.1:c.439-30675_439-30670dup	XM_005244773.1:c.439-30676_439-30670dup
PRDM16 transcript variant X3	XM_005244774.1:c.439-30689=	XM_005244774.1:c.439-30678_439-30670del	XM_005244774.1:c.439-30674_439-30670del	XM_005244774.1:c.439-30673_439-30670del	XM_005244774.1:c.439-30672_439-30670del	XM_005244774.1:c.439-30671_439-30670del	XM_005244774.1:c.439-30670del	XM_005244774.1:c.439-30670dup	XM_005244774.1:c.439-30671_439-30670dup	XM_005244774.1:c.439-30672_439-30670dup	XM_005244774.1:c.439-30673_439-30670dup	XM_005244774.1:c.439-30674_439-30670dup	XM_005244774.1:c.439-30675_439-30670dup	XM_005244774.1:c.439-30676_439-30670dup

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#.

50 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41156349	Oct 11, 2018 (152)
2	HGSV	ss77937553	Oct 11, 2018 (152)
3	HGSV	ss83922111	Dec 15, 2007 (129)
4	HUMANGENOME_JCVI	ss95912679	Oct 11, 2018 (152)
5	PJP	ss294562909	Oct 11, 2018 (152)
6	PJP	ss294562910	Oct 11, 2018 (152)
7	SSMP	ss663181612	Apr 01, 2015 (144)
8	SWEGEN	ss2986194503	Nov 08, 2017 (151)
9	EVA_DECODE	ss3686038756	Jul 12, 2019 (153)
10	EVA_DECODE	ss3686038757	Jul 12, 2019 (153)
11	EVA_DECODE	ss3686038758	Jul 12, 2019 (153)
12	EVA_DECODE	ss3686038759	Jul 12, 2019 (153)
13	EVA_DECODE	ss3686038760	Jul 12, 2019 (153)
14	EVA_DECODE	ss3686038761	Jul 12, 2019 (153)
15	PACBIO	ss3788984810	Jul 12, 2019 (153)
16	PACBIO	ss3793857450	Jul 12, 2019 (153)
17	EVA	ss3825991896	Apr 25, 2020 (154)
18	KRGDB	ss3892919682	Apr 25, 2020 (154)
19	GNOMAD	ss3987308893	Apr 25, 2021 (155)
20	GNOMAD	ss3987308894	Apr 25, 2021 (155)
21	GNOMAD	ss3987308895	Apr 25, 2021 (155)
22	GNOMAD	ss3987308896	Apr 25, 2021 (155)
23	GNOMAD	ss3987308897	Apr 25, 2021 (155)
24	GNOMAD	ss3987308898	Apr 25, 2021 (155)
25	GNOMAD	ss3987308899	Apr 25, 2021 (155)
26	GNOMAD	ss3987308900	Apr 25, 2021 (155)
27	GNOMAD	ss3987308901	Apr 25, 2021 (155)
28	GNOMAD	ss3987308902	Apr 25, 2021 (155)
29	GNOMAD	ss3987308903	Apr 25, 2021 (155)
30	GNOMAD	ss3987308904	Apr 25, 2021 (155)
31	GNOMAD	ss3987308905	Apr 25, 2021 (155)
32	TOMMO_GENOMICS	ss5142181902	Apr 25, 2021 (155)
33	TOMMO_GENOMICS	ss5142181903	Apr 25, 2021 (155)
34	TOMMO_GENOMICS	ss5142181904	Apr 25, 2021 (155)
35	1000G_HIGH_COVERAGE	ss5240952557	Oct 12, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5240952558	Oct 12, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5240952559	Oct 12, 2022 (156)
38	1000G_HIGH_COVERAGE	ss5240952560	Oct 12, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5240952561	Oct 12, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5240952562	Oct 12, 2022 (156)
41	HUGCELL_USP	ss5442180327	Oct 12, 2022 (156)
42	HUGCELL_USP	ss5442180328	Oct 12, 2022 (156)
43	HUGCELL_USP	ss5442180329	Oct 12, 2022 (156)
44	HUGCELL_USP	ss5442180330	Oct 12, 2022 (156)
45	HUGCELL_USP	ss5442180331	Oct 12, 2022 (156)
46	HUGCELL_USP	ss5442180332	Oct 12, 2022 (156)
47	TOMMO_GENOMICS	ss5666388929	Oct 12, 2022 (156)
48	TOMMO_GENOMICS	ss5666388930	Oct 12, 2022 (156)
49	TOMMO_GENOMICS	ss5666388931	Oct 12, 2022 (156)
50	TOMMO_GENOMICS	ss5666388932	Oct 12, 2022 (156)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 750315 (NC_000001.11:3354459::A 46837/104082) Row 750316 (NC_000001.11:3354459::AA 1317/104224) Row 750317 (NC_000001.11:3354459::AAA 965/104262)...	-	Apr 25, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 750315 (NC_000001.11:3354459::A 46837/104082) Row 750316 (NC_000001.11:3354459::AA 1317/104224) Row 750317 (NC_000001.11:3354459::AAA 965/104262)...	-	Apr 25, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 750315 (NC_000001.11:3354459::A 46837/104082) Row 750316 (NC_000001.11:3354459::AA 1317/104224) Row 750317 (NC_000001.11:3354459::AAA 965/104262)...	-	Apr 25, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 750315 (NC_000001.11:3354459::A 46837/104082) Row 750316 (NC_000001.11:3354459::AA 1317/104224) Row 750317 (NC_000001.11:3354459::AAA 965/104262)...	-	Apr 25, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 750315 (NC_000001.11:3354459::A 46837/104082) Row 750316 (NC_000001.11:3354459::AA 1317/104224) Row 750317 (NC_000001.11:3354459::AAA 965/104262)...	-	Apr 25, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 750315 (NC_000001.11:3354459::A 46837/104082) Row 750316 (NC_000001.11:3354459::AA 1317/104224) Row 750317 (NC_000001.11:3354459::AAA 965/104262)...	-	Apr 25, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 750315 (NC_000001.11:3354459::A 46837/104082) Row 750316 (NC_000001.11:3354459::AA 1317/104224) Row 750317 (NC_000001.11:3354459::AAA 965/104262)...	-	Apr 25, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 750315 (NC_000001.11:3354459::A 46837/104082) Row 750316 (NC_000001.11:3354459::AA 1317/104224) Row 750317 (NC_000001.11:3354459::AAA 965/104262)...	-	Apr 25, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 750315 (NC_000001.11:3354459::A 46837/104082) Row 750316 (NC_000001.11:3354459::AA 1317/104224) Row 750317 (NC_000001.11:3354459::AAA 965/104262)...	-	Apr 25, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 750315 (NC_000001.11:3354459::A 46837/104082) Row 750316 (NC_000001.11:3354459::AA 1317/104224) Row 750317 (NC_000001.11:3354459::AAA 965/104262)...	-	Apr 25, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 750315 (NC_000001.11:3354459::A 46837/104082) Row 750316 (NC_000001.11:3354459::AA 1317/104224) Row 750317 (NC_000001.11:3354459::AAA 965/104262)...	-	Apr 25, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 750315 (NC_000001.11:3354459::A 46837/104082) Row 750316 (NC_000001.11:3354459::AA 1317/104224) Row 750317 (NC_000001.11:3354459::AAA 965/104262)...	-	Apr 25, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 750315 (NC_000001.11:3354459::A 46837/104082) Row 750316 (NC_000001.11:3354459::AA 1317/104224) Row 750317 (NC_000001.11:3354459::AAA 965/104262)...	-	Apr 25, 2021 (155)
64	KOREAN population from KRGDB	NC_000001.10 - 3271024	Apr 25, 2020 (154)
65	8.3KJPN Submission ignored due to conflicting rows: Row 151209 (NC_000001.10:3271023::A 5512/16580) Row 151210 (NC_000001.10:3271023::AA 51/16580) Row 151211 (NC_000001.10:3271023:A: 23/16580)	-	Apr 25, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 151209 (NC_000001.10:3271023::A 5512/16580) Row 151210 (NC_000001.10:3271023::AA 51/16580) Row 151211 (NC_000001.10:3271023:A: 23/16580)	-	Apr 25, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 151209 (NC_000001.10:3271023::A 5512/16580) Row 151210 (NC_000001.10:3271023::AA 51/16580) Row 151211 (NC_000001.10:3271023:A: 23/16580)	-	Apr 25, 2021 (155)
68	14KJPN Submission ignored due to conflicting rows: Row 226033 (NC_000001.11:3354459::A 9788/28158) Row 226034 (NC_000001.11:3354459::AA 84/28158) Row 226035 (NC_000001.11:3354459:A: 30/28158)...	-	Oct 12, 2022 (156)
69	14KJPN Submission ignored due to conflicting rows: Row 226033 (NC_000001.11:3354459::A 9788/28158) Row 226034 (NC_000001.11:3354459::AA 84/28158) Row 226035 (NC_000001.11:3354459:A: 30/28158)...	-	Oct 12, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 226033 (NC_000001.11:3354459::A 9788/28158) Row 226034 (NC_000001.11:3354459::AA 84/28158) Row 226035 (NC_000001.11:3354459:A: 30/28158)...	-	Oct 12, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 226033 (NC_000001.11:3354459::A 9788/28158) Row 226034 (NC_000001.11:3354459::AA 84/28158) Row 226035 (NC_000001.11:3354459:A: 30/28158)...	-	Oct 12, 2022 (156)
72	ALFA	NC_000001.11 - 3354460	Apr 25, 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
ss3987308905	NC_000001.11:3354459:AAAAAAAAA:	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
7003508190	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss3987308904	NC_000001.11:3354459:AAAAA:	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
7003508190	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss2986194503	NC_000001.10:3271023:AAAA:	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3987308903	NC_000001.11:3354459:AAAA:	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
7003508190	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss83922111	NC_000001.8:3294197:AAA:	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3686038761, ss3987308902, ss5240952561, ss5442180327	NC_000001.11:3354459:AAA:	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
7003508190	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3987308901, ss5240952559, ss5442180328	NC_000001.11:3354459:AA:	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
7003508190	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3686038760	NC_000001.11:3354460:AA:	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss5142181904	NC_000001.10:3271023:A:	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3987308900, ss5442180329, ss5666388931	NC_000001.11:3354459:A:	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
7003508190	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3686038759	NC_000001.11:3354461:A:	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss294562909	NC_000001.9:3260884::A	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss294562910	NC_000001.9:3260903::A	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
97076, ss663181612, ss3788984810, ss3793857450, ss3825991896, ss3892919682, ss5142181902	NC_000001.10:3271023::A	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3987308893, ss5240952558, ss5442180330, ss5666388929	NC_000001.11:3354459::A	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
7003508190	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3686038758	NC_000001.11:3354462::A	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss41156349	NT_004350.19:2749655::A	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss77937553, ss95912679	NT_004350.19:2749675::A	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss5142181903	NC_000001.10:3271023::AA	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3987308894, ss5240952557, ss5442180331, ss5666388930	NC_000001.11:3354459::AA	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
7003508190	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3686038757	NC_000001.11:3354462::AA	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3987308895, ss5240952562, ss5666388932	NC_000001.11:3354459::AAA	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
7003508190	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3987308896, ss5240952560, ss5442180332	NC_000001.11:3354459::AAAA	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
7003508190	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3987308897	NC_000001.11:3354459::AAAAA	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
7003508190	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3987308898	NC_000001.11:3354459::AAAAAA	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3987308899	NC_000001.11:3354459::AAAAAAA	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3686038756	NC_000001.11:3354462::AAAAAAA	NC_000001.11:3354459:AAAAAAAAAAAAA… NC_000001.11:3354459:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs59791059

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

rs59791059