Name: rs57974422
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.

rs57974422

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr19:23747640-23747661 (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)₈ / del(A)₇ / del(A)₆ / del(…
del(A)₈ / del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dup(A)₅ / dup(A)₁₁ / ins(A)₂₇ / insC(A)₂₄ / insCC(A)₁₄T(A)₂₃
Variation Type: Indel Insertion and Deletion
Frequency: (A)₂₂=0.3548 (1777/5008, 1000G)
del(A)₇=0.00 (0/74, ALFA)
del(A)₆=0.00 (0/74, ALFA) (+ 6 more)
del(A)₅=0.00 (0/74, ALFA)
del(A)₄=0.00 (0/74, ALFA)
delAAA=0.00 (0/74, ALFA)
delAA=0.00 (0/74, ALFA)
delA=0.00 (0/74, ALFA)
dupA=0.00 (0/74, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ZNF681 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

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

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	74	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
European	Sub	62	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African	Sub	10	AAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
African Others	Sub	2	AAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
African American	Sub	8	AAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
East Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	0	AAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 2	Sub	2	AAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
South Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other	Sub	0	AAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A

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

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
1000Genomes	Global	Study-wide	5008	(A)₂₂=0.3548	del(A)₄=0.6452
1000Genomes	African	Sub	1322	(A)₂₂=0.3873	del(A)₄=0.6127
1000Genomes	East Asian	Sub	1008	(A)₂₂=0.1498	del(A)₄=0.8502
1000Genomes	Europe	Sub	1006	(A)₂₂=0.5209	del(A)₄=0.4791
1000Genomes	South Asian	Sub	978	(A)₂₂=0.339	del(A)₄=0.661
1000Genomes	American	Sub	694	(A)₂₂=0.372	del(A)₄=0.628
Allele Frequency Aggregator	Total	Global	74	(A)₂₂=1.00	del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00
Allele Frequency Aggregator	European	Sub	62	(A)₂₂=1.00	del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00
Allele Frequency Aggregator	African	Sub	10	(A)₂₂=1.0	del(A)₇=0.0, del(A)₆=0.0, del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0
Allele Frequency Aggregator	Latin American 2	Sub	2	(A)₂₂=1.0	del(A)₇=0.0, del(A)₆=0.0, del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0
Allele Frequency Aggregator	Latin American 1	Sub	0	(A)₂₂=0	del(A)₇=0, del(A)₆=0, del(A)₅=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0
Allele Frequency Aggregator	South Asian	Sub	0	(A)₂₂=0	del(A)₇=0, del(A)₆=0, del(A)₅=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0
Allele Frequency Aggregator	Other	Sub	0	(A)₂₂=0	del(A)₇=0, del(A)₆=0, del(A)₅=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0
Allele Frequency Aggregator	Asian	Sub	0	(A)₂₂=0	del(A)₇=0, del(A)₆=0, del(A)₅=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0

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

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 19	NC_000019.10:g.23747654_23747661del
GRCh38.p14 chr 19	NC_000019.10:g.23747655_23747661del
GRCh38.p14 chr 19	NC_000019.10:g.23747656_23747661del
GRCh38.p14 chr 19	NC_000019.10:g.23747657_23747661del
GRCh38.p14 chr 19	NC_000019.10:g.23747658_23747661del
GRCh38.p14 chr 19	NC_000019.10:g.23747659_23747661del
GRCh38.p14 chr 19	NC_000019.10:g.23747660_23747661del
GRCh38.p14 chr 19	NC_000019.10:g.23747661del
GRCh38.p14 chr 19	NC_000019.10:g.23747661dup
GRCh38.p14 chr 19	NC_000019.10:g.23747660_23747661dup
GRCh38.p14 chr 19	NC_000019.10:g.23747657_23747661dup
GRCh38.p14 chr 19	NC_000019.10:g.23747651_23747661dup
GRCh38.p14 chr 19	NC_000019.10:g.23747661_23747662insAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 19	NC_000019.10:g.23747640_23747661A[22]CAAAAAAAAAAAAAAAAAAAAAAAA[1]
GRCh38.p14 chr 19	NC_000019.10:g.23747640_23747661A[22]CCAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAA[1]
GRCh37.p13 chr 19	NC_000019.9:g.23930456_23930463del
GRCh37.p13 chr 19	NC_000019.9:g.23930457_23930463del
GRCh37.p13 chr 19	NC_000019.9:g.23930458_23930463del
GRCh37.p13 chr 19	NC_000019.9:g.23930459_23930463del
GRCh37.p13 chr 19	NC_000019.9:g.23930460_23930463del
GRCh37.p13 chr 19	NC_000019.9:g.23930461_23930463del
GRCh37.p13 chr 19	NC_000019.9:g.23930462_23930463del
GRCh37.p13 chr 19	NC_000019.9:g.23930463del
GRCh37.p13 chr 19	NC_000019.9:g.23930463dup
GRCh37.p13 chr 19	NC_000019.9:g.23930462_23930463dup
GRCh37.p13 chr 19	NC_000019.9:g.23930459_23930463dup
GRCh37.p13 chr 19	NC_000019.9:g.23930453_23930463dup
GRCh37.p13 chr 19	NC_000019.9:g.23930463_23930464insAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 19	NC_000019.9:g.23930442_23930463A[22]CAAAAAAAAAAAAAAAAAAAAAAAA[1]
GRCh37.p13 chr 19	NC_000019.9:g.23930442_23930463A[22]CCAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAA[1]

Gene: ZNF681, zinc finger protein 681 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ZNF681 transcript	NM_138286.3:c.227-2324_22… NM_138286.3:c.227-2324_227-2317del	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)₂₂=	del(A)₈	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dup(A)₅	dup(A)₁₁	ins(A)₂₇	insC(A)₂₄	insCC(A)₁₄T(A)₂₃
GRCh38.p14 chr 19	NC_000019.10:g.23747640_23747661=	NC_000019.10:g.23747654_23747661del	NC_000019.10:g.23747655_23747661del	NC_000019.10:g.23747656_23747661del	NC_000019.10:g.23747657_23747661del	NC_000019.10:g.23747658_23747661del	NC_000019.10:g.23747659_23747661del	NC_000019.10:g.23747660_23747661del	NC_000019.10:g.23747661del	NC_000019.10:g.23747661dup	NC_000019.10:g.23747660_23747661dup	NC_000019.10:g.23747657_23747661dup	NC_000019.10:g.23747651_23747661dup	NC_000019.10:g.23747661_23747662insAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000019.10:g.23747640_23747661A[22]CAAAAAAAAAAAAAAAAAAAAAAAA[1]	NC_000019.10:g.23747640_23747661A[22]CCAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAA[1]
GRCh37.p13 chr 19	NC_000019.9:g.23930442_23930463=	NC_000019.9:g.23930456_23930463del	NC_000019.9:g.23930457_23930463del	NC_000019.9:g.23930458_23930463del	NC_000019.9:g.23930459_23930463del	NC_000019.9:g.23930460_23930463del	NC_000019.9:g.23930461_23930463del	NC_000019.9:g.23930462_23930463del	NC_000019.9:g.23930463del	NC_000019.9:g.23930463dup	NC_000019.9:g.23930462_23930463dup	NC_000019.9:g.23930459_23930463dup	NC_000019.9:g.23930453_23930463dup	NC_000019.9:g.23930463_23930464insAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000019.9:g.23930442_23930463A[22]CAAAAAAAAAAAAAAAAAAAAAAAA[1]	NC_000019.9:g.23930442_23930463A[22]CCAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAA[1]
ZNF681 transcript	NM_138286.2:c.227-2317=	NM_138286.2:c.227-2324_227-2317del	NM_138286.2:c.227-2323_227-2317del	NM_138286.2:c.227-2322_227-2317del	NM_138286.2:c.227-2321_227-2317del	NM_138286.2:c.227-2320_227-2317del	NM_138286.2:c.227-2319_227-2317del	NM_138286.2:c.227-2318_227-2317del	NM_138286.2:c.227-2317del	NM_138286.2:c.227-2317dup	NM_138286.2:c.227-2318_227-2317dup	NM_138286.2:c.227-2321_227-2317dup	NM_138286.2:c.227-2327_227-2317dup	NM_138286.2:c.227-2317_227-2316insTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_138286.2:c.227-2317_227-2316insTTTTTTTTTTTTTTTTTTTTTTTTG	NM_138286.2:c.227-2317_227-2316insTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTGG
ZNF681 transcript	NM_138286.3:c.227-2317=	NM_138286.3:c.227-2324_227-2317del	NM_138286.3:c.227-2323_227-2317del	NM_138286.3:c.227-2322_227-2317del	NM_138286.3:c.227-2321_227-2317del	NM_138286.3:c.227-2320_227-2317del	NM_138286.3:c.227-2319_227-2317del	NM_138286.3:c.227-2318_227-2317del	NM_138286.3:c.227-2317del	NM_138286.3:c.227-2317dup	NM_138286.3:c.227-2318_227-2317dup	NM_138286.3:c.227-2321_227-2317dup	NM_138286.3:c.227-2327_227-2317dup	NM_138286.3:c.227-2317_227-2316insTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_138286.3:c.227-2317_227-2316insTTTTTTTTTTTTTTTTTTTTTTTTG	NM_138286.3:c.227-2317_227-2316insTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTGG
ZNF681 transcript variant X1	XM_005259766.1:c.206-2317=	XM_005259766.1:c.206-2324_206-2317del	XM_005259766.1:c.206-2323_206-2317del	XM_005259766.1:c.206-2322_206-2317del	XM_005259766.1:c.206-2321_206-2317del	XM_005259766.1:c.206-2320_206-2317del	XM_005259766.1:c.206-2319_206-2317del	XM_005259766.1:c.206-2318_206-2317del	XM_005259766.1:c.206-2317del	XM_005259766.1:c.206-2317dup	XM_005259766.1:c.206-2318_206-2317dup	XM_005259766.1:c.206-2321_206-2317dup	XM_005259766.1:c.206-2327_206-2317dup	XM_005259766.1:c.206-2317_206-2316insTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005259766.1:c.206-2317_206-2316insTTTTTTTTTTTTTTTTTTTTTTTTG	XM_005259766.1:c.206-2317_206-2316insTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTGG
ZNF681 transcript variant X2	XM_005259767.1:c.20-2317=	XM_005259767.1:c.20-2324_20-2317del	XM_005259767.1:c.20-2323_20-2317del	XM_005259767.1:c.20-2322_20-2317del	XM_005259767.1:c.20-2321_20-2317del	XM_005259767.1:c.20-2320_20-2317del	XM_005259767.1:c.20-2319_20-2317del	XM_005259767.1:c.20-2318_20-2317del	XM_005259767.1:c.20-2317del	XM_005259767.1:c.20-2317dup	XM_005259767.1:c.20-2318_20-2317dup	XM_005259767.1:c.20-2321_20-2317dup	XM_005259767.1:c.20-2327_20-2317dup	XM_005259767.1:c.20-2317_20-2316insTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005259767.1:c.20-2317_20-2316insTTTTTTTTTTTTTTTTTTTTTTTTG	XM_005259767.1:c.20-2317_20-2316insTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTGG
ZNF681 transcript variant X3	XM_005259768.1:c.20-2317=	XM_005259768.1:c.20-2324_20-2317del	XM_005259768.1:c.20-2323_20-2317del	XM_005259768.1:c.20-2322_20-2317del	XM_005259768.1:c.20-2321_20-2317del	XM_005259768.1:c.20-2320_20-2317del	XM_005259768.1:c.20-2319_20-2317del	XM_005259768.1:c.20-2318_20-2317del	XM_005259768.1:c.20-2317del	XM_005259768.1:c.20-2317dup	XM_005259768.1:c.20-2318_20-2317dup	XM_005259768.1:c.20-2321_20-2317dup	XM_005259768.1:c.20-2327_20-2317dup	XM_005259768.1:c.20-2317_20-2316insTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005259768.1:c.20-2317_20-2316insTTTTTTTTTTTTTTTTTTTTTTTTG	XM_005259768.1:c.20-2317_20-2316insTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTGG
ZNF681 transcript variant X4	XM_005259769.1:c.227-2317=	XM_005259769.1:c.227-2324_227-2317del	XM_005259769.1:c.227-2323_227-2317del	XM_005259769.1:c.227-2322_227-2317del	XM_005259769.1:c.227-2321_227-2317del	XM_005259769.1:c.227-2320_227-2317del	XM_005259769.1:c.227-2319_227-2317del	XM_005259769.1:c.227-2318_227-2317del	XM_005259769.1:c.227-2317del	XM_005259769.1:c.227-2317dup	XM_005259769.1:c.227-2318_227-2317dup	XM_005259769.1:c.227-2321_227-2317dup	XM_005259769.1:c.227-2327_227-2317dup	XM_005259769.1:c.227-2317_227-2316insTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005259769.1:c.227-2317_227-2316insTTTTTTTTTTTTTTTTTTTTTTTTG	XM_005259769.1:c.227-2317_227-2316insTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTGG
ZNF681 transcript variant X5	XM_005259770.1:c.227-2317=	XM_005259770.1:c.227-2324_227-2317del	XM_005259770.1:c.227-2323_227-2317del	XM_005259770.1:c.227-2322_227-2317del	XM_005259770.1:c.227-2321_227-2317del	XM_005259770.1:c.227-2320_227-2317del	XM_005259770.1:c.227-2319_227-2317del	XM_005259770.1:c.227-2318_227-2317del	XM_005259770.1:c.227-2317del	XM_005259770.1:c.227-2317dup	XM_005259770.1:c.227-2318_227-2317dup	XM_005259770.1:c.227-2321_227-2317dup	XM_005259770.1:c.227-2327_227-2317dup	XM_005259770.1:c.227-2317_227-2316insTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005259770.1:c.227-2317_227-2316insTTTTTTTTTTTTTTTTTTTTTTTTG	XM_005259770.1:c.227-2317_227-2316insTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTGG

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#.

70 SubSNP, 32 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80905751	Dec 15, 2007 (129)
2	HGSV	ss82774336	Dec 14, 2007 (129)
3	HUMANGENOME_JCVI	ss95725602	Mar 15, 2016 (147)
4	HUMANGENOME_JCVI	ss96279532	Feb 16, 2009 (130)
5	1000GENOMES	ss1378058765	Aug 21, 2014 (142)
6	EVA_UK10K_ALSPAC	ss1709163772	Apr 01, 2015 (144)
7	EVA_UK10K_TWINSUK	ss1709168678	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1710786503	Apr 01, 2015 (144)
9	EVA_UK10K_ALSPAC	ss1710786504	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1710786505	Apr 01, 2015 (144)
11	EVA_UK10K_ALSPAC	ss1710786506	Apr 01, 2015 (144)
12	SWEGEN	ss3017285699	Nov 08, 2017 (151)
13	MCHAISSO	ss3063912144	Nov 08, 2017 (151)
14	MCHAISSO	ss3064759837	Nov 08, 2017 (151)
15	MCHAISSO	ss3064759838	Nov 08, 2017 (151)
16	MCHAISSO	ss3065707803	Nov 08, 2017 (151)
17	MCHAISSO	ss3065707804	Nov 08, 2017 (151)
18	URBANLAB	ss3650894371	Oct 12, 2018 (152)
19	EVA_DECODE	ss3702561183	Jul 13, 2019 (153)
20	EVA_DECODE	ss3702561184	Jul 13, 2019 (153)
21	EVA_DECODE	ss3702561185	Jul 13, 2019 (153)
22	EVA_DECODE	ss3702561186	Jul 13, 2019 (153)
23	EVA_DECODE	ss3702561187	Jul 13, 2019 (153)
24	ACPOP	ss3742949875	Jul 13, 2019 (153)
25	ACPOP	ss3742949876	Jul 13, 2019 (153)
26	ACPOP	ss3742949877	Jul 13, 2019 (153)
27	ACPOP	ss3742949878	Jul 13, 2019 (153)
28	PACBIO	ss3788501575	Jul 13, 2019 (153)
29	PACBIO	ss3793416569	Jul 13, 2019 (153)
30	PACBIO	ss3793416570	Jul 13, 2019 (153)
31	PACBIO	ss3798303427	Jul 13, 2019 (153)
32	PACBIO	ss3798303428	Jul 13, 2019 (153)
33	KHV_HUMAN_GENOMES	ss3821191478	Jul 13, 2019 (153)
34	EVA	ss3835409738	Apr 27, 2020 (154)
35	GNOMAD	ss4329484006	Apr 26, 2021 (155)
36	GNOMAD	ss4329484007	Apr 26, 2021 (155)
37	GNOMAD	ss4329484008	Apr 26, 2021 (155)
38	GNOMAD	ss4329484009	Apr 26, 2021 (155)
39	GNOMAD	ss4329484010	Apr 26, 2021 (155)
40	GNOMAD	ss4329484011	Apr 26, 2021 (155)
41	GNOMAD	ss4329484012	Apr 26, 2021 (155)
42	GNOMAD	ss4329484013	Apr 26, 2021 (155)
43	GNOMAD	ss4329484014	Apr 26, 2021 (155)
44	GNOMAD	ss4329484015	Apr 26, 2021 (155)
45	GNOMAD	ss4329484016	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5227256507	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5227256508	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5227256509	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5227256510	Apr 26, 2021 (155)
50	TOMMO_GENOMICS	ss5227256511	Apr 26, 2021 (155)
51	1000G_HIGH_COVERAGE	ss5306880151	Oct 16, 2022 (156)
52	1000G_HIGH_COVERAGE	ss5306880152	Oct 16, 2022 (156)
53	1000G_HIGH_COVERAGE	ss5306880153	Oct 16, 2022 (156)
54	1000G_HIGH_COVERAGE	ss5306880154	Oct 16, 2022 (156)
55	1000G_HIGH_COVERAGE	ss5306880155	Oct 16, 2022 (156)
56	HUGCELL_USP	ss5499455578	Oct 16, 2022 (156)
57	HUGCELL_USP	ss5499455579	Oct 16, 2022 (156)
58	HUGCELL_USP	ss5499455580	Oct 16, 2022 (156)
59	HUGCELL_USP	ss5499455581	Oct 16, 2022 (156)
60	HUGCELL_USP	ss5499455582	Oct 16, 2022 (156)
61	TOMMO_GENOMICS	ss5785717853	Oct 16, 2022 (156)
62	TOMMO_GENOMICS	ss5785717854	Oct 16, 2022 (156)
63	TOMMO_GENOMICS	ss5785717855	Oct 16, 2022 (156)
64	TOMMO_GENOMICS	ss5785717856	Oct 16, 2022 (156)
65	TOMMO_GENOMICS	ss5785717857	Oct 16, 2022 (156)
66	EVA	ss5840405595	Oct 16, 2022 (156)
67	EVA	ss5840405596	Oct 16, 2022 (156)
68	EVA	ss5840405597	Oct 16, 2022 (156)
69	EVA	ss5927700088	Oct 16, 2022 (156)
70	EVA	ss5981044043	Oct 16, 2022 (156)
71	1000Genomes	NC_000019.9 - 23930442	Oct 12, 2018 (152)
72	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 42180637 (NC_000019.9:23930442:AA: 1176/3854) Row 42180639 (NC_000019.9:23930441:AAAA: 1004/3854)	-	Oct 12, 2018 (152)
73	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 42180637 (NC_000019.9:23930442:AA: 1176/3854) Row 42180639 (NC_000019.9:23930441:AAAA: 1004/3854)	-	Oct 12, 2018 (152)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 537060432 (NC_000019.10:23747639::A 23/87972) Row 537060433 (NC_000019.10:23747639::AA 4/88002) Row 537060434 (NC_000019.10:23747639::AAAAA 1/88012)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 537060432 (NC_000019.10:23747639::A 23/87972) Row 537060433 (NC_000019.10:23747639::AA 4/88002) Row 537060434 (NC_000019.10:23747639::AAAAA 1/88012)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 537060432 (NC_000019.10:23747639::A 23/87972) Row 537060433 (NC_000019.10:23747639::AA 4/88002) Row 537060434 (NC_000019.10:23747639::AAAAA 1/88012)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 537060432 (NC_000019.10:23747639::A 23/87972) Row 537060433 (NC_000019.10:23747639::AA 4/88002) Row 537060434 (NC_000019.10:23747639::AAAAA 1/88012)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 537060432 (NC_000019.10:23747639::A 23/87972) Row 537060433 (NC_000019.10:23747639::AA 4/88002) Row 537060434 (NC_000019.10:23747639::AAAAA 1/88012)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 537060432 (NC_000019.10:23747639::A 23/87972) Row 537060433 (NC_000019.10:23747639::AA 4/88002) Row 537060434 (NC_000019.10:23747639::AAAAA 1/88012)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 537060432 (NC_000019.10:23747639::A 23/87972) Row 537060433 (NC_000019.10:23747639::AA 4/88002) Row 537060434 (NC_000019.10:23747639::AAAAA 1/88012)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 537060432 (NC_000019.10:23747639::A 23/87972) Row 537060433 (NC_000019.10:23747639::AA 4/88002) Row 537060434 (NC_000019.10:23747639::AAAAA 1/88012)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 537060432 (NC_000019.10:23747639::A 23/87972) Row 537060433 (NC_000019.10:23747639::AA 4/88002) Row 537060434 (NC_000019.10:23747639::AAAAA 1/88012)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 537060432 (NC_000019.10:23747639::A 23/87972) Row 537060433 (NC_000019.10:23747639::AA 4/88002) Row 537060434 (NC_000019.10:23747639::AAAAA 1/88012)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 537060432 (NC_000019.10:23747639::A 23/87972) Row 537060433 (NC_000019.10:23747639::AA 4/88002) Row 537060434 (NC_000019.10:23747639::AAAAA 1/88012)...	-	Apr 26, 2021 (155)
85	Northern Sweden Submission ignored due to conflicting rows: Row 16234740 (NC_000019.9:23930441:A: 79/486) Row 16234741 (NC_000019.9:23930441:AAA: 7/486) Row 16234742 (NC_000019.9:23930441:AAAA: 28/486)...	-	Jul 13, 2019 (153)
86	Northern Sweden Submission ignored due to conflicting rows: Row 16234740 (NC_000019.9:23930441:A: 79/486) Row 16234741 (NC_000019.9:23930441:AAA: 7/486) Row 16234742 (NC_000019.9:23930441:AAAA: 28/486)...	-	Jul 13, 2019 (153)
87	Northern Sweden Submission ignored due to conflicting rows: Row 16234740 (NC_000019.9:23930441:A: 79/486) Row 16234741 (NC_000019.9:23930441:AAA: 7/486) Row 16234742 (NC_000019.9:23930441:AAAA: 28/486)...	-	Jul 13, 2019 (153)
88	Northern Sweden Submission ignored due to conflicting rows: Row 16234740 (NC_000019.9:23930441:A: 79/486) Row 16234741 (NC_000019.9:23930441:AAA: 7/486) Row 16234742 (NC_000019.9:23930441:AAAA: 28/486)...	-	Jul 13, 2019 (153)
89	8.3KJPN Submission ignored due to conflicting rows: Row 85225814 (NC_000019.9:23930441:AA: 2967/16524) Row 85225815 (NC_000019.9:23930441:A: 1956/16524) Row 85225816 (NC_000019.9:23930441:AAAA: 6986/16524)...	-	Apr 26, 2021 (155)
90	8.3KJPN Submission ignored due to conflicting rows: Row 85225814 (NC_000019.9:23930441:AA: 2967/16524) Row 85225815 (NC_000019.9:23930441:A: 1956/16524) Row 85225816 (NC_000019.9:23930441:AAAA: 6986/16524)...	-	Apr 26, 2021 (155)
91	8.3KJPN Submission ignored due to conflicting rows: Row 85225814 (NC_000019.9:23930441:AA: 2967/16524) Row 85225815 (NC_000019.9:23930441:A: 1956/16524) Row 85225816 (NC_000019.9:23930441:AAAA: 6986/16524)...	-	Apr 26, 2021 (155)
92	8.3KJPN Submission ignored due to conflicting rows: Row 85225814 (NC_000019.9:23930441:AA: 2967/16524) Row 85225815 (NC_000019.9:23930441:A: 1956/16524) Row 85225816 (NC_000019.9:23930441:AAAA: 6986/16524)...	-	Apr 26, 2021 (155)
93	8.3KJPN Submission ignored due to conflicting rows: Row 85225814 (NC_000019.9:23930441:AA: 2967/16524) Row 85225815 (NC_000019.9:23930441:A: 1956/16524) Row 85225816 (NC_000019.9:23930441:AAAA: 6986/16524)...	-	Apr 26, 2021 (155)
94	14KJPN Submission ignored due to conflicting rows: Row 119554957 (NC_000019.10:23747639:AAAA: 12881/28112) Row 119554958 (NC_000019.10:23747639:AA: 5411/28112) Row 119554959 (NC_000019.10:23747639:AAAAA: 654/28112)...	-	Oct 16, 2022 (156)
95	14KJPN Submission ignored due to conflicting rows: Row 119554957 (NC_000019.10:23747639:AAAA: 12881/28112) Row 119554958 (NC_000019.10:23747639:AA: 5411/28112) Row 119554959 (NC_000019.10:23747639:AAAAA: 654/28112)...	-	Oct 16, 2022 (156)
96	14KJPN Submission ignored due to conflicting rows: Row 119554957 (NC_000019.10:23747639:AAAA: 12881/28112) Row 119554958 (NC_000019.10:23747639:AA: 5411/28112) Row 119554959 (NC_000019.10:23747639:AAAAA: 654/28112)...	-	Oct 16, 2022 (156)
97	14KJPN Submission ignored due to conflicting rows: Row 119554957 (NC_000019.10:23747639:AAAA: 12881/28112) Row 119554958 (NC_000019.10:23747639:AA: 5411/28112) Row 119554959 (NC_000019.10:23747639:AAAAA: 654/28112)...	-	Oct 16, 2022 (156)
98	14KJPN Submission ignored due to conflicting rows: Row 119554957 (NC_000019.10:23747639:AAAA: 12881/28112) Row 119554958 (NC_000019.10:23747639:AA: 5411/28112) Row 119554959 (NC_000019.10:23747639:AAAAA: 654/28112)...	-	Oct 16, 2022 (156)
99	UK 10K study - Twins Submission ignored due to conflicting rows: Row 42180637 (NC_000019.9:23930442:AA: 1094/3708) Row 42180639 (NC_000019.9:23930441:AAAA: 1011/3708)	-	Oct 12, 2018 (152)
100	UK 10K study - Twins Submission ignored due to conflicting rows: Row 42180637 (NC_000019.9:23930442:AAA: 1094/3708) Row 42180638 (NC_000019.9:23930443:AA: 1584/3708) Row 42180639 (NC_000019.9:23930441:AAAA: 1011/3708)	-	Apr 27, 2020 (154)
101	UK 10K study - Twins Submission ignored due to conflicting rows: Row 42180637 (NC_000019.9:23930442:AA: 1094/3708) Row 42180639 (NC_000019.9:23930441:AAAA: 1011/3708)	-	Oct 12, 2018 (152)
102	ALFA	NC_000019.10 - 23747640	Apr 26, 2021 (155)

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

Associated ID	History Updated (Build)
rs71165890	Oct 15, 2011 (136)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4329484016	NC_000019.10:23747639:AAAAAAAA:	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4329484015	NC_000019.10:23747639:AAAAAAA:	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
11733951823	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4329484014	NC_000019.10:23747639:AAAAAA:	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
11733951823	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss5227256511	NC_000019.9:23930441:AAAAA:	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3702561187, ss4329484013, ss5306880155, ss5499455581, ss5785717855, ss5927700088	NC_000019.10:23747639:AAAAA:	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
11733951823	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
76150389, ss1378058765, ss1709163772, ss1709168678, ss3017285699, ss3742949877, ss3788501575, ss3793416569, ss3798303427, ss5227256509, ss5840405597, ss5981044043	NC_000019.9:23930441:AAAA:	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3063912144, ss3064759837, ss3065707804, ss3821191478, ss5306880151, ss5499455582, ss5785717853	NC_000019.10:23747639:AAAA:	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
11733951823	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3702561186	NC_000019.10:23747640:AAAA:	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss82774336	NC_000019.8:23722300:AAA:	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3742949876, ss3793416570, ss3798303428, ss5227256510, ss5840405596	NC_000019.9:23930441:AAA:	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss1710786503, ss1710786504	NC_000019.9:23930442:AAA:	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3064759838, ss3065707803, ss5306880153, ss5499455580, ss5785717856	NC_000019.10:23747639:AAA:	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
11733951823	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3702561185	NC_000019.10:23747641:AAA:	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3742949878, ss5227256507, ss5840405595	NC_000019.9:23930441:AA:	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
	NC_000019.9:23930442:AA:	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss1710786505, ss1710786506	NC_000019.9:23930443:AA:	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss5306880154, ss5499455579, ss5785717854	NC_000019.10:23747639:AA:	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
11733951823	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3702561184	NC_000019.10:23747642:AA:	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss95725602	NT_011295.11:15193263:AA:	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss80905751	NC_000019.8:23722302:A:	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3742949875, ss3835409738, ss5227256508	NC_000019.9:23930441:A:	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3650894371, ss5306880152, ss5499455578, ss5785717857	NC_000019.10:23747639:A:	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
11733951823	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3702561183	NC_000019.10:23747643:A:	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss96279532	NT_011295.11:15193243:A:	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4329484006	NC_000019.10:23747639::A	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
11733951823	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4329484007	NC_000019.10:23747639::AA	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4329484008	NC_000019.10:23747639::AAAAA	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4329484009	NC_000019.10:23747639::AAAAAAAAAAA	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4329484010	NC_000019.10:23747639::AAAAAAAAAAA… NC_000019.10:23747639::AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4329484011	NC_000019.10:23747639::AAAAAAAAAAA… NC_000019.10:23747639::AAAAAAAAAAAAAAAAAAAAAACAA	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4329484012	NC_000019.10:23747639::AAAAAAAAAAA… NC_000019.10:23747639::AAAAAAAAAAAAAAAAAAAAAACCAAAAAAAAAAAAAATA	NC_000019.10:23747639:AAAAAAAAAAAA… NC_000019.10:23747639:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAACCAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAA	(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 rs57974422

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

rs57974422