Name: rs71580638
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.

rs71580638

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:114576223-114576248 (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(CT)₇ / del(CT)₆ / del(CT)₅ / d…
del(CT)₇ / del(CT)₆ / del(CT)₅ / del(CT)₄ / del(CT)₃ / delCTCT / delCT / dupCT / dupCTCT / dup(CT)₃ / dup(CT)₄ / dup(CT)₅ / dup(CT)₆
Variation Type: Indel Insertion and Deletion
Frequency: dupCT=0.09143 (1067/11670, ALFA)
dupCT=0.28 (11/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: BCAS2 : 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	11670	CTCTCTCTCTCTCTCTCTCTCTCTCT=0.89794	CTCTCTCTCTCTCTCT=0.00206, CTCTCTCTCTCTCTCTCT=0.00000, CTCTCTCTCTCTCTCTCTCT=0.00000, CTCTCTCTCTCTCTCTCTCTCT=0.00000, CTCTCTCTCTCTCTCTCTCTCTCT=0.00420, CTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.09143, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00386, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00051, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00000, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00000	0.84287	0.023972	0.133158	32
European	Sub	8358	CTCTCTCTCTCTCTCTCTCTCTCTCT=0.8577	CTCTCTCTCTCTCTCT=0.0029, CTCTCTCTCTCTCTCTCT=0.0000, CTCTCTCTCTCTCTCTCTCT=0.0000, CTCTCTCTCTCTCTCTCTCTCT=0.0000, CTCTCTCTCTCTCTCTCTCTCTCT=0.0059, CTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.1274, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0054, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0007, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0000, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0000	0.779256	0.033752	0.186992	32
African	Sub	2288	CTCTCTCTCTCTCTCTCTCTCTCTCT=1.0000	CTCTCTCTCTCTCTCT=0.0000, CTCTCTCTCTCTCTCTCT=0.0000, CTCTCTCTCTCTCTCTCTCT=0.0000, CTCTCTCTCTCTCTCTCTCTCT=0.0000, CTCTCTCTCTCTCTCTCTCTCTCT=0.0000, CTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0000, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0000, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0000, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0000, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	96	CTCTCTCTCTCTCTCTCTCTCTCTCT=1.00	CTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00	1.0	0.0	0.0	N/A
African American	Sub	2192	CTCTCTCTCTCTCTCTCTCTCTCTCT=1.0000	CTCTCTCTCTCTCTCT=0.0000, CTCTCTCTCTCTCTCTCT=0.0000, CTCTCTCTCTCTCTCTCTCT=0.0000, CTCTCTCTCTCTCTCTCTCTCT=0.0000, CTCTCTCTCTCTCTCTCTCTCTCT=0.0000, CTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0000, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0000, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0000, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0000, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	104	CTCTCTCTCTCTCTCTCTCTCTCTCT=1.000	CTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000	1.0	0.0	0.0	N/A
East Asian	Sub	80	CTCTCTCTCTCTCTCTCTCTCTCTCT=1.00	CTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	24	CTCTCTCTCTCTCTCTCTCTCTCTCT=1.00	CTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	106	CTCTCTCTCTCTCTCTCTCTCTCTCT=1.000	CTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000	1.0	0.0	0.0	N/A
Latin American 2	Sub	442	CTCTCTCTCTCTCTCTCTCTCTCTCT=1.000	CTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	66	CTCTCTCTCTCTCTCTCTCTCTCTCT=1.00	CTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.00	1.0	0.0	0.0	N/A
Other	Sub	306	CTCTCTCTCTCTCTCTCTCTCTCTCT=0.993	CTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.007, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000, CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT=0.000	0.986928	0.0	0.013072	0

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	11670	(CT)₁₃=0.89794	del(CT)₅=0.00206, del(CT)₄=0.00000, del(CT)₃=0.00000, delCTCT=0.00000, delCT=0.00420, dupCT=0.09143, dupCTCT=0.00386, dup(CT)₃=0.00051, dup(CT)₄=0.00000, dup(CT)₆=0.00000
Allele Frequency Aggregator	European	Sub	8358	(CT)₁₃=0.8577	del(CT)₅=0.0029, del(CT)₄=0.0000, del(CT)₃=0.0000, delCTCT=0.0000, delCT=0.0059, dupCT=0.1274, dupCTCT=0.0054, dup(CT)₃=0.0007, dup(CT)₄=0.0000, dup(CT)₆=0.0000
Allele Frequency Aggregator	African	Sub	2288	(CT)₁₃=1.0000	del(CT)₅=0.0000, del(CT)₄=0.0000, del(CT)₃=0.0000, delCTCT=0.0000, delCT=0.0000, dupCT=0.0000, dupCTCT=0.0000, dup(CT)₃=0.0000, dup(CT)₄=0.0000, dup(CT)₆=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	442	(CT)₁₃=1.000	del(CT)₅=0.000, del(CT)₄=0.000, del(CT)₃=0.000, delCTCT=0.000, delCT=0.000, dupCT=0.000, dupCTCT=0.000, dup(CT)₃=0.000, dup(CT)₄=0.000, dup(CT)₆=0.000
Allele Frequency Aggregator	Other	Sub	306	(CT)₁₃=0.993	del(CT)₅=0.000, del(CT)₄=0.000, del(CT)₃=0.000, delCTCT=0.000, delCT=0.000, dupCT=0.007, dupCTCT=0.000, dup(CT)₃=0.000, dup(CT)₄=0.000, dup(CT)₆=0.000
Allele Frequency Aggregator	Latin American 1	Sub	106	(CT)₁₃=1.000	del(CT)₅=0.000, del(CT)₄=0.000, del(CT)₃=0.000, delCTCT=0.000, delCT=0.000, dupCT=0.000, dupCTCT=0.000, dup(CT)₃=0.000, dup(CT)₄=0.000, dup(CT)₆=0.000
Allele Frequency Aggregator	Asian	Sub	104	(CT)₁₃=1.000	del(CT)₅=0.000, del(CT)₄=0.000, del(CT)₃=0.000, delCTCT=0.000, delCT=0.000, dupCT=0.000, dupCTCT=0.000, dup(CT)₃=0.000, dup(CT)₄=0.000, dup(CT)₆=0.000
Allele Frequency Aggregator	South Asian	Sub	66	(CT)₁₃=1.00	del(CT)₅=0.00, del(CT)₄=0.00, del(CT)₃=0.00, delCTCT=0.00, delCT=0.00, dupCT=0.00, dupCTCT=0.00, dup(CT)₃=0.00, dup(CT)₄=0.00, dup(CT)₆=0.00
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupCT=0.28

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.114576223CT[6]
GRCh38.p14 chr 1	NC_000001.11:g.114576223CT[7]
GRCh38.p14 chr 1	NC_000001.11:g.114576223CT[8]
GRCh38.p14 chr 1	NC_000001.11:g.114576223CT[9]
GRCh38.p14 chr 1	NC_000001.11:g.114576223CT[10]
GRCh38.p14 chr 1	NC_000001.11:g.114576223CT[11]
GRCh38.p14 chr 1	NC_000001.11:g.114576223CT[12]
GRCh38.p14 chr 1	NC_000001.11:g.114576223CT[14]
GRCh38.p14 chr 1	NC_000001.11:g.114576223CT[15]
GRCh38.p14 chr 1	NC_000001.11:g.114576223CT[16]
GRCh38.p14 chr 1	NC_000001.11:g.114576223CT[17]
GRCh38.p14 chr 1	NC_000001.11:g.114576223CT[18]
GRCh38.p14 chr 1	NC_000001.11:g.114576223CT[19]
GRCh37.p13 chr 1	NC_000001.10:g.115118844CT[6]
GRCh37.p13 chr 1	NC_000001.10:g.115118844CT[7]
GRCh37.p13 chr 1	NC_000001.10:g.115118844CT[8]
GRCh37.p13 chr 1	NC_000001.10:g.115118844CT[9]
GRCh37.p13 chr 1	NC_000001.10:g.115118844CT[10]
GRCh37.p13 chr 1	NC_000001.10:g.115118844CT[11]
GRCh37.p13 chr 1	NC_000001.10:g.115118844CT[12]
GRCh37.p13 chr 1	NC_000001.10:g.115118844CT[14]
GRCh37.p13 chr 1	NC_000001.10:g.115118844CT[15]
GRCh37.p13 chr 1	NC_000001.10:g.115118844CT[16]
GRCh37.p13 chr 1	NC_000001.10:g.115118844CT[17]
GRCh37.p13 chr 1	NC_000001.10:g.115118844CT[18]
GRCh37.p13 chr 1	NC_000001.10:g.115118844CT[19]

Gene: BCAS2, BCAS2 pre-mRNA processing factor (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
BCAS2 transcript	NM_005872.3:c.257+440AG[6]	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	(CT)₁₃=	del(CT)₇	del(CT)₆	del(CT)₅	del(CT)₄	del(CT)₃	delCTCT	delCT	dupCT	dupCTCT	dup(CT)₃	dup(CT)₄	dup(CT)₅	dup(CT)₆
GRCh38.p14 chr 1	NC_000001.11:g.114576223_114576248=	NC_000001.11:g.114576223CT[6]	NC_000001.11:g.114576223CT[7]	NC_000001.11:g.114576223CT[8]	NC_000001.11:g.114576223CT[9]	NC_000001.11:g.114576223CT[10]	NC_000001.11:g.114576223CT[11]	NC_000001.11:g.114576223CT[12]	NC_000001.11:g.114576223CT[14]	NC_000001.11:g.114576223CT[15]	NC_000001.11:g.114576223CT[16]	NC_000001.11:g.114576223CT[17]	NC_000001.11:g.114576223CT[18]	NC_000001.11:g.114576223CT[19]
GRCh37.p13 chr 1	NC_000001.10:g.115118844_115118869=	NC_000001.10:g.115118844CT[6]	NC_000001.10:g.115118844CT[7]	NC_000001.10:g.115118844CT[8]	NC_000001.10:g.115118844CT[9]	NC_000001.10:g.115118844CT[10]	NC_000001.10:g.115118844CT[11]	NC_000001.10:g.115118844CT[12]	NC_000001.10:g.115118844CT[14]	NC_000001.10:g.115118844CT[15]	NC_000001.10:g.115118844CT[16]	NC_000001.10:g.115118844CT[17]	NC_000001.10:g.115118844CT[18]	NC_000001.10:g.115118844CT[19]
BCAS2 transcript	NM_005872.2:c.257+465=	NM_005872.2:c.257+440AG[6]	NM_005872.2:c.257+440AG[7]	NM_005872.2:c.257+440AG[8]	NM_005872.2:c.257+440AG[9]	NM_005872.2:c.257+440AG[10]	NM_005872.2:c.257+440AG[11]	NM_005872.2:c.257+440AG[12]	NM_005872.2:c.257+440AG[14]	NM_005872.2:c.257+440AG[15]	NM_005872.2:c.257+440AG[16]	NM_005872.2:c.257+440AG[17]	NM_005872.2:c.257+440AG[18]	NM_005872.2:c.257+440AG[19]
BCAS2 transcript	NM_005872.3:c.257+465=	NM_005872.3:c.257+440AG[6]	NM_005872.3:c.257+440AG[7]	NM_005872.3:c.257+440AG[8]	NM_005872.3:c.257+440AG[9]	NM_005872.3:c.257+440AG[10]	NM_005872.3:c.257+440AG[11]	NM_005872.3:c.257+440AG[12]	NM_005872.3:c.257+440AG[14]	NM_005872.3:c.257+440AG[15]	NM_005872.3:c.257+440AG[16]	NM_005872.3:c.257+440AG[17]	NM_005872.3:c.257+440AG[18]	NM_005872.3:c.257+440AG[19]
BCAS2 transcript variant X1	XM_005270349.1:c.-73-472=	XM_005270349.1:c.-73-497AG[6]	XM_005270349.1:c.-73-497AG[7]	XM_005270349.1:c.-73-497AG[8]	XM_005270349.1:c.-73-497AG[9]	XM_005270349.1:c.-73-497AG[10]	XM_005270349.1:c.-73-497AG[11]	XM_005270349.1:c.-73-497AG[12]	XM_005270349.1:c.-73-497AG[14]	XM_005270349.1:c.-73-497AG[15]	XM_005270349.1:c.-73-497AG[16]	XM_005270349.1:c.-73-497AG[17]	XM_005270349.1:c.-73-497AG[18]	XM_005270349.1:c.-73-497AG[19]

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#.

60 SubSNP, 30 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41151424	Oct 11, 2018 (152)
2	HUMANGENOME_JCVI	ss98575600	Feb 13, 2009 (130)
3	SSMP	ss663111786	Apr 01, 2015 (144)
4	EVA_GENOME_DK	ss1574011211	Apr 01, 2015 (144)
5	EVA_UK10K_ALSPAC	ss1701138039	Apr 01, 2015 (144)
6	EVA_UK10K_ALSPAC	ss1701138042	Apr 01, 2015 (144)
7	EVA_UK10K_TWINSUK	ss1701138424	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1701138428	Apr 01, 2015 (144)
9	SWEGEN	ss2987475685	Nov 08, 2017 (151)
10	MCHAISSO	ss3064419940	Nov 08, 2017 (151)
11	EVA_DECODE	ss3687575491	Jul 12, 2019 (153)
12	EVA_DECODE	ss3687575492	Jul 12, 2019 (153)
13	EVA_DECODE	ss3687575493	Jul 12, 2019 (153)
14	EVA_DECODE	ss3687575494	Jul 12, 2019 (153)
15	EVA_DECODE	ss3687575495	Jul 12, 2019 (153)
16	EVA_DECODE	ss3687575496	Jul 12, 2019 (153)
17	ACPOP	ss3727408286	Jul 12, 2019 (153)
18	ACPOP	ss3727408287	Jul 12, 2019 (153)
19	ACPOP	ss3727408288	Jul 12, 2019 (153)
20	PACBIO	ss3783525800	Jul 12, 2019 (153)
21	PACBIO	ss3789166544	Jul 12, 2019 (153)
22	PACBIO	ss3794039487	Jul 12, 2019 (153)
23	EVA	ss3826381721	Apr 25, 2020 (154)
24	EVA	ss3836582263	Apr 25, 2020 (154)
25	EVA	ss3841990723	Apr 25, 2020 (154)
26	GNOMAD	ss4000838717	Apr 25, 2021 (155)
27	GNOMAD	ss4000838718	Apr 25, 2021 (155)
28	GNOMAD	ss4000838719	Apr 25, 2021 (155)
29	GNOMAD	ss4000838720	Apr 25, 2021 (155)
30	GNOMAD	ss4000838721	Apr 25, 2021 (155)
31	GNOMAD	ss4000838722	Apr 25, 2021 (155)
32	GNOMAD	ss4000838723	Apr 25, 2021 (155)
33	GNOMAD	ss4000838724	Apr 25, 2021 (155)
34	GNOMAD	ss4000838725	Apr 25, 2021 (155)
35	GNOMAD	ss4000838726	Apr 25, 2021 (155)
36	GNOMAD	ss4000838727	Apr 25, 2021 (155)
37	TOMMO_GENOMICS	ss5145783515	Apr 25, 2021 (155)
38	TOMMO_GENOMICS	ss5145783516	Apr 25, 2021 (155)
39	TOMMO_GENOMICS	ss5145783517	Apr 25, 2021 (155)
40	TOMMO_GENOMICS	ss5145783518	Apr 25, 2021 (155)
41	TOMMO_GENOMICS	ss5145783519	Apr 25, 2021 (155)
42	1000G_HIGH_COVERAGE	ss5243687547	Oct 12, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5243687548	Oct 12, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5243687549	Oct 12, 2022 (156)
45	1000G_HIGH_COVERAGE	ss5243687550	Oct 12, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5243687551	Oct 12, 2022 (156)
47	1000G_HIGH_COVERAGE	ss5243687552	Oct 12, 2022 (156)
48	HUGCELL_USP	ss5444603424	Oct 12, 2022 (156)
49	HUGCELL_USP	ss5444603425	Oct 12, 2022 (156)
50	HUGCELL_USP	ss5444603426	Oct 12, 2022 (156)
51	HUGCELL_USP	ss5444603427	Oct 12, 2022 (156)
52	HUGCELL_USP	ss5444603428	Oct 12, 2022 (156)
53	TOMMO_GENOMICS	ss5671082961	Oct 12, 2022 (156)
54	TOMMO_GENOMICS	ss5671082962	Oct 12, 2022 (156)
55	TOMMO_GENOMICS	ss5671082963	Oct 12, 2022 (156)
56	TOMMO_GENOMICS	ss5671082964	Oct 12, 2022 (156)
57	TOMMO_GENOMICS	ss5671082965	Oct 12, 2022 (156)
58	EVA	ss5832514436	Oct 12, 2022 (156)
59	EVA	ss5832514437	Oct 12, 2022 (156)
60	EVA	ss5832514438	Oct 12, 2022 (156)
61	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 1827466 (NC_000001.10:115118843::CT 1151/3854) Row 1827467 (NC_000001.10:115118843::CTCT 52/3854)	-	Oct 11, 2018 (152)
62	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 1827466 (NC_000001.10:115118843::CT 1151/3854) Row 1827467 (NC_000001.10:115118843::CTCT 52/3854)	-	Oct 11, 2018 (152)
63	The Danish reference pan genome	NC_000001.10 - 115118844	Apr 25, 2020 (154)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 23356416 (NC_000001.11:114576222::CT 20955/123696) Row 23356417 (NC_000001.11:114576222::CTCT 744/124114) Row 23356418 (NC_000001.11:114576222::CTCTCT 216/124174)...	-	Apr 25, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 23356416 (NC_000001.11:114576222::CT 20955/123696) Row 23356417 (NC_000001.11:114576222::CTCT 744/124114) Row 23356418 (NC_000001.11:114576222::CTCTCT 216/124174)...	-	Apr 25, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 23356416 (NC_000001.11:114576222::CT 20955/123696) Row 23356417 (NC_000001.11:114576222::CTCT 744/124114) Row 23356418 (NC_000001.11:114576222::CTCTCT 216/124174)...	-	Apr 25, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 23356416 (NC_000001.11:114576222::CT 20955/123696) Row 23356417 (NC_000001.11:114576222::CTCT 744/124114) Row 23356418 (NC_000001.11:114576222::CTCTCT 216/124174)...	-	Apr 25, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 23356416 (NC_000001.11:114576222::CT 20955/123696) Row 23356417 (NC_000001.11:114576222::CTCT 744/124114) Row 23356418 (NC_000001.11:114576222::CTCTCT 216/124174)...	-	Apr 25, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 23356416 (NC_000001.11:114576222::CT 20955/123696) Row 23356417 (NC_000001.11:114576222::CTCT 744/124114) Row 23356418 (NC_000001.11:114576222::CTCTCT 216/124174)...	-	Apr 25, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 23356416 (NC_000001.11:114576222::CT 20955/123696) Row 23356417 (NC_000001.11:114576222::CTCT 744/124114) Row 23356418 (NC_000001.11:114576222::CTCTCT 216/124174)...	-	Apr 25, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 23356416 (NC_000001.11:114576222::CT 20955/123696) Row 23356417 (NC_000001.11:114576222::CTCT 744/124114) Row 23356418 (NC_000001.11:114576222::CTCTCT 216/124174)...	-	Apr 25, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 23356416 (NC_000001.11:114576222::CT 20955/123696) Row 23356417 (NC_000001.11:114576222::CTCT 744/124114) Row 23356418 (NC_000001.11:114576222::CTCTCT 216/124174)...	-	Apr 25, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 23356416 (NC_000001.11:114576222::CT 20955/123696) Row 23356417 (NC_000001.11:114576222::CTCT 744/124114) Row 23356418 (NC_000001.11:114576222::CTCTCT 216/124174)...	-	Apr 25, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 23356416 (NC_000001.11:114576222::CT 20955/123696) Row 23356417 (NC_000001.11:114576222::CTCT 744/124114) Row 23356418 (NC_000001.11:114576222::CTCTCT 216/124174)...	-	Apr 25, 2021 (155)
75	Northern Sweden Submission ignored due to conflicting rows: Row 693151 (NC_000001.10:115118843::CT 132/600) Row 693152 (NC_000001.10:115118843::CTCT 8/600) Row 693153 (NC_000001.10:115118843:CTCTCTCTCT: 2/600)	-	Jul 12, 2019 (153)
76	Northern Sweden Submission ignored due to conflicting rows: Row 693151 (NC_000001.10:115118843::CT 132/600) Row 693152 (NC_000001.10:115118843::CTCT 8/600) Row 693153 (NC_000001.10:115118843:CTCTCTCTCT: 2/600)	-	Jul 12, 2019 (153)
77	Northern Sweden Submission ignored due to conflicting rows: Row 693151 (NC_000001.10:115118843::CT 132/600) Row 693152 (NC_000001.10:115118843::CTCT 8/600) Row 693153 (NC_000001.10:115118843:CTCTCTCTCT: 2/600)	-	Jul 12, 2019 (153)
78	8.3KJPN Submission ignored due to conflicting rows: Row 3752822 (NC_000001.10:115118843:CT: 109/16760) Row 3752823 (NC_000001.10:115118843::CT 85/16760) Row 3752824 (NC_000001.10:115118843:CTCT: 9/16760)...	-	Apr 25, 2021 (155)
79	8.3KJPN Submission ignored due to conflicting rows: Row 3752822 (NC_000001.10:115118843:CT: 109/16760) Row 3752823 (NC_000001.10:115118843::CT 85/16760) Row 3752824 (NC_000001.10:115118843:CTCT: 9/16760)...	-	Apr 25, 2021 (155)
80	8.3KJPN Submission ignored due to conflicting rows: Row 3752822 (NC_000001.10:115118843:CT: 109/16760) Row 3752823 (NC_000001.10:115118843::CT 85/16760) Row 3752824 (NC_000001.10:115118843:CTCT: 9/16760)...	-	Apr 25, 2021 (155)
81	8.3KJPN Submission ignored due to conflicting rows: Row 3752822 (NC_000001.10:115118843:CT: 109/16760) Row 3752823 (NC_000001.10:115118843::CT 85/16760) Row 3752824 (NC_000001.10:115118843:CTCT: 9/16760)...	-	Apr 25, 2021 (155)
82	8.3KJPN Submission ignored due to conflicting rows: Row 3752822 (NC_000001.10:115118843:CT: 109/16760) Row 3752823 (NC_000001.10:115118843::CT 85/16760) Row 3752824 (NC_000001.10:115118843:CTCT: 9/16760)...	-	Apr 25, 2021 (155)
83	14KJPN Submission ignored due to conflicting rows: Row 4920065 (NC_000001.11:114576222:CT: 115/28256) Row 4920066 (NC_000001.11:114576222:CTCT: 10/28256) Row 4920067 (NC_000001.11:114576222::CT 146/28256)...	-	Oct 12, 2022 (156)
84	14KJPN Submission ignored due to conflicting rows: Row 4920065 (NC_000001.11:114576222:CT: 115/28256) Row 4920066 (NC_000001.11:114576222:CTCT: 10/28256) Row 4920067 (NC_000001.11:114576222::CT 146/28256)...	-	Oct 12, 2022 (156)
85	14KJPN Submission ignored due to conflicting rows: Row 4920065 (NC_000001.11:114576222:CT: 115/28256) Row 4920066 (NC_000001.11:114576222:CTCT: 10/28256) Row 4920067 (NC_000001.11:114576222::CT 146/28256)...	-	Oct 12, 2022 (156)
86	14KJPN Submission ignored due to conflicting rows: Row 4920065 (NC_000001.11:114576222:CT: 115/28256) Row 4920066 (NC_000001.11:114576222:CTCT: 10/28256) Row 4920067 (NC_000001.11:114576222::CT 146/28256)...	-	Oct 12, 2022 (156)
87	14KJPN Submission ignored due to conflicting rows: Row 4920065 (NC_000001.11:114576222:CT: 115/28256) Row 4920066 (NC_000001.11:114576222:CTCT: 10/28256) Row 4920067 (NC_000001.11:114576222::CT 146/28256)...	-	Oct 12, 2022 (156)
88	UK 10K study - Twins Submission ignored due to conflicting rows: Row 1827466 (NC_000001.10:115118843::CT 1102/3708) Row 1827467 (NC_000001.10:115118843::CTCT 31/3708)	-	Oct 11, 2018 (152)
89	UK 10K study - Twins Submission ignored due to conflicting rows: Row 1827466 (NC_000001.10:115118843::CT 1102/3708) Row 1827467 (NC_000001.10:115118843::CTCT 31/3708)	-	Oct 11, 2018 (152)
90	ALFA	NC_000001.11 - 114576223	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
ss5145783519	NC_000001.10:115118843:CTCTCTCTCTC… NC_000001.10:115118843:CTCTCTCTCTCTCT:	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCT	(self)
ss5671082965	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCT:	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCT
ss2987475685	NC_000001.10:115118843:CTCTCTCTCTC… NC_000001.10:115118843:CTCTCTCTCTCT:	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCT	(self)
ss3727408288	NC_000001.10:115118843:CTCTCTCTCT:	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCT	(self)
ss4000838727, ss5243687552, ss5444603428	NC_000001.11:114576222:CTCTCTCTCT:	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCT	(self)
4108208621	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCT	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCT	(self)
ss4000838726	NC_000001.11:114576222:CTCTCTCT:	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCT	(self)
4108208621	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCT	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCT	(self)
ss5832514438	NC_000001.10:115118843:CTCTCT:	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCT
ss3687575496, ss4000838725, ss5243687549	NC_000001.11:114576222:CTCTCT:	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCT	(self)
4108208621	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCT	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCT	(self)
ss5145783517	NC_000001.10:115118843:CTCT:	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCT	(self)
ss4000838724, ss5671082962	NC_000001.11:114576222:CTCT:	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCT	(self)
4108208621	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCT	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCT	(self)
ss3687575495	NC_000001.11:114576224:CTCT:	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCT	(self)
ss5145783515, ss5832514437	NC_000001.10:115118843:CT:	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss4000838723, ss5243687547, ss5444603424, ss5671082961	NC_000001.11:114576222:CT:	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCTCT	(self)
4108208621	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCTCT	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss3687575494	NC_000001.11:114576226:CT:	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCTCT	(self)
167676, ss663111786, ss1574011211, ss1701138039, ss1701138424, ss3727408286, ss3783525800, ss3789166544, ss3794039487, ss3826381721, ss3836582263, ss5145783516, ss5832514436	NC_000001.10:115118843::CT	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss3064419940, ss3841990723, ss4000838717, ss5243687548, ss5444603425, ss5671082963	NC_000001.11:114576222::CT	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
4108208621	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCTCTCTCT	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss3687575493	NC_000001.11:114576228::CT	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss98575600	NT_032977.9:85090761::CT	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss41151424	NT_032977.9:85090762::TC	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss1701138042, ss1701138428, ss3727408287, ss5145783518	NC_000001.10:115118843::CTCT	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss4000838718, ss5243687550, ss5444603426, ss5671082964	NC_000001.11:114576222::CTCT	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
4108208621	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss3687575492	NC_000001.11:114576228::CTCT	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss4000838719, ss5243687551, ss5444603427	NC_000001.11:114576222::CTCTCT	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
4108208621	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss3687575491	NC_000001.11:114576228::CTCTCT	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss4000838720	NC_000001.11:114576222::CTCTCTCT	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
4108208621	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss4000838721	NC_000001.11:114576222::CTCTCTCTCT	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
ss4000838722	NC_000001.11:114576222::CTCTCTCTCT… NC_000001.11:114576222::CTCTCTCTCTCT	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(self)
4108208621	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	NC_000001.11:114576222:CTCTCTCTCTC… NC_000001.11:114576222:CTCTCTCTCTCTCTCTCTCTCTCTCT:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT	(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 rs71580638

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

Genome context:

Select flank length:

Genomic regions, transcripts, and products
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs71580638