Name: rs33944071
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.

rs33944071

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:67489198-67489222 (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(CA)₆ / del(CA)₅ / del(CA)₄ / d…
del(CA)₆ / del(CA)₅ / del(CA)₄ / del(CA)₃ / delCACA / delCA / dupCA / dupCACA / dup(CA)₃ / dup(CA)₄ / dup(CA)₅ / dup(CA)₆
Variation Type: Indel Insertion and Deletion
Frequency: (AC)₁₂A=0.1373 (680/4952, ALFA)
delCACA=0.0537 (207/3854, ALSPAC)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CENPC : 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	4952	ACACACACACACACACACACACACA=0.1373	ACACACACACACA=0.0000, ACACACACACACACA=0.0000, ACACACACACACACACA=0.0000, ACACACACACACACACACA=0.0000, ACACACACACACACACACACA=0.0010, ACACACACACACACACACACACA=0.8148, ACACACACACACACACACACACACACACA=0.0208, ACACACACACACACACACACACACACA=0.0261, ACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACACA=0.0000	0.108192	0.808994	0.082814	32
European	Sub	4518	ACACACACACACACACACACACACA=0.0562	ACACACACACACA=0.0000, ACACACACACACACA=0.0000, ACACACACACACACACA=0.0000, ACACACACACACACACACA=0.0000, ACACACACACACACACACACA=0.0011, ACACACACACACACACACACACA=0.8915, ACACACACACACACACACACACACACACA=0.0226, ACACACACACACACACACACACACACA=0.0286, ACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACACA=0.0000	0.014778	0.893596	0.091626	32
African	Sub	366	ACACACACACACACACACACACACA=1.000	ACACACACACACA=0.000, ACACACACACACACA=0.000, ACACACACACACACACA=0.000, ACACACACACACACACACA=0.000, ACACACACACACACACACACA=0.000, ACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	22	ACACACACACACACACACACACACA=1.00	ACACACACACACA=0.00, ACACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
African American	Sub	344	ACACACACACACACACACACACACA=1.000	ACACACACACACA=0.000, ACACACACACACACA=0.000, ACACACACACACACACA=0.000, ACACACACACACACACACA=0.000, ACACACACACACACACACACA=0.000, ACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACACA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	16	ACACACACACACACACACACACACA=1.00	ACACACACACACA=0.00, ACACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	14	ACACACACACACACACACACACACA=1.00	ACACACACACACA=0.00, ACACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	2	ACACACACACACACACACACACACA=1.0	ACACACACACACA=0.0, ACACACACACACACA=0.0, ACACACACACACACACA=0.0, ACACACACACACACACACA=0.0, ACACACACACACACACACACA=0.0, ACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACACACACA=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	10	ACACACACACACACACACACACACA=1.0	ACACACACACACA=0.0, ACACACACACACACA=0.0, ACACACACACACACACA=0.0, ACACACACACACACACACA=0.0, ACACACACACACACACACACA=0.0, ACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACACACACA=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	10	ACACACACACACACACACACACACA=1.0	ACACACACACACA=0.0, ACACACACACACACA=0.0, ACACACACACACACACA=0.0, ACACACACACACACACACA=0.0, ACACACACACACACACACACA=0.0, ACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACACACACACA=0.0	1.0	0.0	0.0	N/A
South Asian	Sub	0	ACACACACACACACACACACACACA=0	ACACACACACACA=0, ACACACACACACACA=0, ACACACACACACACACA=0, ACACACACACACACACACA=0, ACACACACACACACACACACA=0, ACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACACACACA=0, ACACACACACACACACACACACACACACACACACACA=0	0	0	0	N/A
Other	Sub	32	ACACACACACACACACACACACACA=0.75	ACACACACACACA=0.00, ACACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.22, ACACACACACACACACACACACACACACA=0.03, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACACA=0.00	0.8	0.2	0.0	9

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	4952	(AC)₁₂A=0.1373	del(CA)₆=0.0000, del(CA)₅=0.0000, del(CA)₄=0.0000, del(CA)₃=0.0000, delCACA=0.0010, delCA=0.8148, dupCA=0.0261, dupCACA=0.0208, dup(CA)₃=0.0000, dup(CA)₄=0.0000, dup(CA)₅=0.0000, dup(CA)₆=0.0000
Allele Frequency Aggregator	European	Sub	4518	(AC)₁₂A=0.0562	del(CA)₆=0.0000, del(CA)₅=0.0000, del(CA)₄=0.0000, del(CA)₃=0.0000, delCACA=0.0011, delCA=0.8915, dupCA=0.0286, dupCACA=0.0226, dup(CA)₃=0.0000, dup(CA)₄=0.0000, dup(CA)₅=0.0000, dup(CA)₆=0.0000
Allele Frequency Aggregator	African	Sub	366	(AC)₁₂A=1.000	del(CA)₆=0.000, del(CA)₅=0.000, del(CA)₄=0.000, del(CA)₃=0.000, delCACA=0.000, delCA=0.000, dupCA=0.000, dupCACA=0.000, dup(CA)₃=0.000, dup(CA)₄=0.000, dup(CA)₅=0.000, dup(CA)₆=0.000
Allele Frequency Aggregator	Other	Sub	32	(AC)₁₂A=0.75	del(CA)₆=0.00, del(CA)₅=0.00, del(CA)₄=0.00, del(CA)₃=0.00, delCACA=0.00, delCA=0.22, dupCA=0.00, dupCACA=0.03, dup(CA)₃=0.00, dup(CA)₄=0.00, dup(CA)₅=0.00, dup(CA)₆=0.00
Allele Frequency Aggregator	Asian	Sub	16	(AC)₁₂A=1.00	del(CA)₆=0.00, del(CA)₅=0.00, del(CA)₄=0.00, del(CA)₃=0.00, delCACA=0.00, delCA=0.00, dupCA=0.00, dupCACA=0.00, dup(CA)₃=0.00, dup(CA)₄=0.00, dup(CA)₅=0.00, dup(CA)₆=0.00
Allele Frequency Aggregator	Latin American 1	Sub	10	(AC)₁₂A=1.0	del(CA)₆=0.0, del(CA)₅=0.0, del(CA)₄=0.0, del(CA)₃=0.0, delCACA=0.0, delCA=0.0, dupCA=0.0, dupCACA=0.0, dup(CA)₃=0.0, dup(CA)₄=0.0, dup(CA)₅=0.0, dup(CA)₆=0.0
Allele Frequency Aggregator	Latin American 2	Sub	10	(AC)₁₂A=1.0	del(CA)₆=0.0, del(CA)₅=0.0, del(CA)₄=0.0, del(CA)₃=0.0, delCACA=0.0, delCA=0.0, dupCA=0.0, dupCACA=0.0, dup(CA)₃=0.0, dup(CA)₄=0.0, dup(CA)₅=0.0, dup(CA)₆=0.0
Allele Frequency Aggregator	South Asian	Sub	0	(AC)₁₂A=0	del(CA)₆=0, del(CA)₅=0, del(CA)₄=0, del(CA)₃=0, delCACA=0, delCA=0, dupCA=0, dupCACA=0, dup(CA)₃=0, dup(CA)₄=0, dup(CA)₅=0, dup(CA)₆=0
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(AC)₁₂A=0.9463	delCACA=0.0537

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 4	NC_000004.12:g.67489199CA[6]
GRCh38.p14 chr 4	NC_000004.12:g.67489199CA[7]
GRCh38.p14 chr 4	NC_000004.12:g.67489199CA[8]
GRCh38.p14 chr 4	NC_000004.12:g.67489199CA[9]
GRCh38.p14 chr 4	NC_000004.12:g.67489199CA[10]
GRCh38.p14 chr 4	NC_000004.12:g.67489199CA[11]
GRCh38.p14 chr 4	NC_000004.12:g.67489199CA[13]
GRCh38.p14 chr 4	NC_000004.12:g.67489199CA[14]
GRCh38.p14 chr 4	NC_000004.12:g.67489199CA[15]
GRCh38.p14 chr 4	NC_000004.12:g.67489199CA[16]
GRCh38.p14 chr 4	NC_000004.12:g.67489199CA[17]
GRCh38.p14 chr 4	NC_000004.12:g.67489199CA[18]
GRCh37.p13 chr 4	NC_000004.11:g.68354917CA[6]
GRCh37.p13 chr 4	NC_000004.11:g.68354917CA[7]
GRCh37.p13 chr 4	NC_000004.11:g.68354917CA[8]
GRCh37.p13 chr 4	NC_000004.11:g.68354917CA[9]
GRCh37.p13 chr 4	NC_000004.11:g.68354917CA[10]
GRCh37.p13 chr 4	NC_000004.11:g.68354917CA[11]
GRCh37.p13 chr 4	NC_000004.11:g.68354917CA[13]
GRCh37.p13 chr 4	NC_000004.11:g.68354917CA[14]
GRCh37.p13 chr 4	NC_000004.11:g.68354917CA[15]
GRCh37.p13 chr 4	NC_000004.11:g.68354917CA[16]
GRCh37.p13 chr 4	NC_000004.11:g.68354917CA[17]
GRCh37.p13 chr 4	NC_000004.11:g.68354917CA[18]

Gene: CENPC, centromere protein C (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CENPC transcript variant 2	NM_001362481.2:c.2646+746… NM_001362481.2:c.2646+746GT[6]	N/A	Intron Variant
CENPC transcript variant 1	NM_001812.4:c.2670+746GT[… NM_001812.4:c.2670+746GT[6]	N/A	Intron Variant
CENPC transcript variant 3	NR_155754.2:n.	N/A	Intron Variant
CENPC transcript variant X1	XM_047449526.1:c.2670+746… XM_047449526.1:c.2670+746GT[6]	N/A	Intron Variant
CENPC transcript variant X2	XM_011531542.4:c.	N/A	Genic Downstream Transcript Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(AC)₁₂A=	del(CA)₆	del(CA)₅	del(CA)₄	del(CA)₃	delCACA	delCA	dupCA	dupCACA	dup(CA)₃	dup(CA)₄	dup(CA)₅	dup(CA)₆
GRCh38.p14 chr 4	NC_000004.12:g.67489198_67489222=	NC_000004.12:g.67489199CA[6]	NC_000004.12:g.67489199CA[7]	NC_000004.12:g.67489199CA[8]	NC_000004.12:g.67489199CA[9]	NC_000004.12:g.67489199CA[10]	NC_000004.12:g.67489199CA[11]	NC_000004.12:g.67489199CA[13]	NC_000004.12:g.67489199CA[14]	NC_000004.12:g.67489199CA[15]	NC_000004.12:g.67489199CA[16]	NC_000004.12:g.67489199CA[17]	NC_000004.12:g.67489199CA[18]
GRCh37.p13 chr 4	NC_000004.11:g.68354916_68354940=	NC_000004.11:g.68354917CA[6]	NC_000004.11:g.68354917CA[7]	NC_000004.11:g.68354917CA[8]	NC_000004.11:g.68354917CA[9]	NC_000004.11:g.68354917CA[10]	NC_000004.11:g.68354917CA[11]	NC_000004.11:g.68354917CA[13]	NC_000004.11:g.68354917CA[14]	NC_000004.11:g.68354917CA[15]	NC_000004.11:g.68354917CA[16]	NC_000004.11:g.68354917CA[17]	NC_000004.11:g.68354917CA[18]
CENPC transcript variant 2	NM_001362481.2:c.2646+769=	NM_001362481.2:c.2646+746GT[6]	NM_001362481.2:c.2646+746GT[7]	NM_001362481.2:c.2646+746GT[8]	NM_001362481.2:c.2646+746GT[9]	NM_001362481.2:c.2646+746GT[10]	NM_001362481.2:c.2646+746GT[11]	NM_001362481.2:c.2646+746GT[13]	NM_001362481.2:c.2646+746GT[14]	NM_001362481.2:c.2646+746GT[15]	NM_001362481.2:c.2646+746GT[16]	NM_001362481.2:c.2646+746GT[17]	NM_001362481.2:c.2646+746GT[18]
CENPC transcript	NM_001812.2:c.2670+769=	NM_001812.2:c.2670+746GT[6]	NM_001812.2:c.2670+746GT[7]	NM_001812.2:c.2670+746GT[8]	NM_001812.2:c.2670+746GT[9]	NM_001812.2:c.2670+746GT[10]	NM_001812.2:c.2670+746GT[11]	NM_001812.2:c.2670+746GT[13]	NM_001812.2:c.2670+746GT[14]	NM_001812.2:c.2670+746GT[15]	NM_001812.2:c.2670+746GT[16]	NM_001812.2:c.2670+746GT[17]	NM_001812.2:c.2670+746GT[18]
CENPC transcript variant 1	NM_001812.4:c.2670+769=	NM_001812.4:c.2670+746GT[6]	NM_001812.4:c.2670+746GT[7]	NM_001812.4:c.2670+746GT[8]	NM_001812.4:c.2670+746GT[9]	NM_001812.4:c.2670+746GT[10]	NM_001812.4:c.2670+746GT[11]	NM_001812.4:c.2670+746GT[13]	NM_001812.4:c.2670+746GT[14]	NM_001812.4:c.2670+746GT[15]	NM_001812.4:c.2670+746GT[16]	NM_001812.4:c.2670+746GT[17]	NM_001812.4:c.2670+746GT[18]
CENPC transcript variant X1	XM_047449526.1:c.2670+769=	XM_047449526.1:c.2670+746GT[6]	XM_047449526.1:c.2670+746GT[7]	XM_047449526.1:c.2670+746GT[8]	XM_047449526.1:c.2670+746GT[9]	XM_047449526.1:c.2670+746GT[10]	XM_047449526.1:c.2670+746GT[11]	XM_047449526.1:c.2670+746GT[13]	XM_047449526.1:c.2670+746GT[14]	XM_047449526.1:c.2670+746GT[15]	XM_047449526.1:c.2670+746GT[16]	XM_047449526.1:c.2670+746GT[17]	XM_047449526.1:c.2670+746GT[18]

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#.

77 SubSNP, 37 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42225639	Mar 14, 2006 (126)
2	HGSV	ss79995813	Sep 08, 2015 (146)
3	HGSV	ss80182810	Sep 08, 2015 (146)
4	HUMANGENOME_JCVI	ss95357685	Feb 05, 2009 (137)
5	BUSHMAN	ss193741894	Jul 04, 2010 (137)
6	GMI	ss287749464	May 09, 2011 (134)
7	GMI	ss288536096	May 04, 2012 (137)
8	GMI	ss288536098	Jan 10, 2018 (151)
9	PJP	ss295169823	May 09, 2011 (137)
10	PJP	ss295169824	May 09, 2011 (137)
11	LUNTER	ss551371672	Apr 25, 2013 (138)
12	BILGI_BIOE	ss666262221	Apr 25, 2013 (138)
13	DDI	ss1536411113	Apr 01, 2015 (144)
14	EVA_UK10K_ALSPAC	ss1704192402	Apr 01, 2015 (144)
15	EVA_UK10K_TWINSUK	ss1704193936	Apr 01, 2015 (144)
16	EVA_UK10K_TWINSUK	ss1710151159	Apr 01, 2015 (144)
17	EVA_UK10K_ALSPAC	ss1710151189	Apr 01, 2015 (144)
18	SWEGEN	ss2994841884	Nov 08, 2017 (151)
19	MCHAISSO	ss3064105757	Nov 08, 2017 (151)
20	MCHAISSO	ss3064972676	Nov 08, 2017 (151)
21	MCHAISSO	ss3065954171	Nov 08, 2017 (151)
22	URBANLAB	ss3647751518	Oct 12, 2018 (152)
23	EVA_DECODE	ss3712219481	Jul 13, 2019 (153)
24	EVA_DECODE	ss3712219482	Jul 13, 2019 (153)
25	EVA_DECODE	ss3712219483	Jul 13, 2019 (153)
26	EVA_DECODE	ss3712219484	Jul 13, 2019 (153)
27	EVA_DECODE	ss3712219485	Jul 13, 2019 (153)
28	EVA_DECODE	ss3712219486	Jul 13, 2019 (153)
29	ACPOP	ss3731226910	Jul 13, 2019 (153)
30	ACPOP	ss3731226911	Jul 13, 2019 (153)
31	ACPOP	ss3731226912	Jul 13, 2019 (153)
32	PACBIO	ss3784738270	Jul 13, 2019 (153)
33	PACBIO	ss3790193119	Jul 13, 2019 (153)
34	PACBIO	ss3795068224	Jul 13, 2019 (153)
35	KHV_HUMAN_GENOMES	ss3805042044	Jul 13, 2019 (153)
36	EVA	ss3828587158	Apr 26, 2020 (154)
37	EVA	ss3837733412	Apr 26, 2020 (154)
38	EVA	ss3843170290	Apr 26, 2020 (154)
39	KOGIC	ss3954343363	Apr 26, 2020 (154)
40	KOGIC	ss3954343364	Apr 26, 2020 (154)
41	KOGIC	ss3954343365	Apr 26, 2020 (154)
42	KOGIC	ss3954343366	Apr 26, 2020 (154)
43	KOGIC	ss3954343367	Apr 26, 2020 (154)
44	GNOMAD	ss4112794723	Apr 26, 2021 (155)
45	GNOMAD	ss4112794724	Apr 26, 2021 (155)
46	GNOMAD	ss4112794725	Apr 26, 2021 (155)
47	GNOMAD	ss4112794726	Apr 26, 2021 (155)
48	GNOMAD	ss4112794727	Apr 26, 2021 (155)
49	GNOMAD	ss4112794728	Apr 26, 2021 (155)
50	GNOMAD	ss4112794729	Apr 26, 2021 (155)
51	GNOMAD	ss4112794730	Apr 26, 2021 (155)
52	GNOMAD	ss4112794731	Apr 26, 2021 (155)
53	GNOMAD	ss4112794732	Apr 26, 2021 (155)
54	TOMMO_GENOMICS	ss5166098543	Apr 26, 2021 (155)
55	TOMMO_GENOMICS	ss5166098544	Apr 26, 2021 (155)
56	TOMMO_GENOMICS	ss5166098545	Apr 26, 2021 (155)
57	TOMMO_GENOMICS	ss5166098546	Apr 26, 2021 (155)
58	TOMMO_GENOMICS	ss5166098547	Apr 26, 2021 (155)
59	TOMMO_GENOMICS	ss5166098548	Apr 26, 2021 (155)
60	1000G_HIGH_COVERAGE	ss5259509119	Oct 13, 2022 (156)
61	1000G_HIGH_COVERAGE	ss5259509120	Oct 13, 2022 (156)
62	1000G_HIGH_COVERAGE	ss5259509121	Oct 13, 2022 (156)
63	1000G_HIGH_COVERAGE	ss5259509122	Oct 13, 2022 (156)
64	1000G_HIGH_COVERAGE	ss5259509123	Oct 13, 2022 (156)
65	1000G_HIGH_COVERAGE	ss5259509124	Oct 13, 2022 (156)
66	HUGCELL_USP	ss5458234946	Oct 13, 2022 (156)
67	HUGCELL_USP	ss5458234947	Oct 13, 2022 (156)
68	HUGCELL_USP	ss5458234948	Oct 13, 2022 (156)
69	TOMMO_GENOMICS	ss5700548259	Oct 13, 2022 (156)
70	TOMMO_GENOMICS	ss5700548260	Oct 13, 2022 (156)
71	TOMMO_GENOMICS	ss5700548261	Oct 13, 2022 (156)
72	TOMMO_GENOMICS	ss5700548262	Oct 13, 2022 (156)
73	TOMMO_GENOMICS	ss5700548263	Oct 13, 2022 (156)
74	TOMMO_GENOMICS	ss5700548264	Oct 13, 2022 (156)
75	EVA	ss5844115476	Oct 13, 2022 (156)
76	EVA	ss5844115477	Oct 13, 2022 (156)
77	EVA	ss5863784737	Oct 13, 2022 (156)
78	The Avon Longitudinal Study of Parents and Children	NC_000004.11 - 68354916	Oct 12, 2018 (152)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 152290104 (NC_000004.12:67489197::AC 5744/136684) Row 152290105 (NC_000004.12:67489197::ACAC 2258/136714) Row 152290106 (NC_000004.12:67489197::ACACAC 41/136768)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 152290104 (NC_000004.12:67489197::AC 5744/136684) Row 152290105 (NC_000004.12:67489197::ACAC 2258/136714) Row 152290106 (NC_000004.12:67489197::ACACAC 41/136768)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 152290104 (NC_000004.12:67489197::AC 5744/136684) Row 152290105 (NC_000004.12:67489197::ACAC 2258/136714) Row 152290106 (NC_000004.12:67489197::ACACAC 41/136768)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 152290104 (NC_000004.12:67489197::AC 5744/136684) Row 152290105 (NC_000004.12:67489197::ACAC 2258/136714) Row 152290106 (NC_000004.12:67489197::ACACAC 41/136768)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 152290104 (NC_000004.12:67489197::AC 5744/136684) Row 152290105 (NC_000004.12:67489197::ACAC 2258/136714) Row 152290106 (NC_000004.12:67489197::ACACAC 41/136768)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 152290104 (NC_000004.12:67489197::AC 5744/136684) Row 152290105 (NC_000004.12:67489197::ACAC 2258/136714) Row 152290106 (NC_000004.12:67489197::ACACAC 41/136768)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 152290104 (NC_000004.12:67489197::AC 5744/136684) Row 152290105 (NC_000004.12:67489197::ACAC 2258/136714) Row 152290106 (NC_000004.12:67489197::ACACAC 41/136768)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 152290104 (NC_000004.12:67489197::AC 5744/136684) Row 152290105 (NC_000004.12:67489197::ACAC 2258/136714) Row 152290106 (NC_000004.12:67489197::ACACAC 41/136768)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 152290104 (NC_000004.12:67489197::AC 5744/136684) Row 152290105 (NC_000004.12:67489197::ACAC 2258/136714) Row 152290106 (NC_000004.12:67489197::ACACAC 41/136768)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 152290104 (NC_000004.12:67489197::AC 5744/136684) Row 152290105 (NC_000004.12:67489197::ACAC 2258/136714) Row 152290106 (NC_000004.12:67489197::ACACAC 41/136768)...	-	Apr 26, 2021 (155)
89	Korean Genome Project Submission ignored due to conflicting rows: Row 10721364 (NC_000004.12:67489199:AC: 555/1832) Row 10721365 (NC_000004.12:67489201::AC 374/1832) Row 10721366 (NC_000004.12:67489201::ACACAC 6/1832)...	-	Apr 26, 2020 (154)
90	Korean Genome Project Submission ignored due to conflicting rows: Row 10721364 (NC_000004.12:67489199:AC: 555/1832) Row 10721365 (NC_000004.12:67489201::AC 374/1832) Row 10721366 (NC_000004.12:67489201::ACACAC 6/1832)...	-	Apr 26, 2020 (154)
91	Korean Genome Project Submission ignored due to conflicting rows: Row 10721364 (NC_000004.12:67489199:AC: 555/1832) Row 10721365 (NC_000004.12:67489201::AC 374/1832) Row 10721366 (NC_000004.12:67489201::ACACAC 6/1832)...	-	Apr 26, 2020 (154)
92	Korean Genome Project Submission ignored due to conflicting rows: Row 10721364 (NC_000004.12:67489199:AC: 555/1832) Row 10721365 (NC_000004.12:67489201::AC 374/1832) Row 10721366 (NC_000004.12:67489201::ACACAC 6/1832)...	-	Apr 26, 2020 (154)
93	Korean Genome Project Submission ignored due to conflicting rows: Row 10721364 (NC_000004.12:67489199:AC: 555/1832) Row 10721365 (NC_000004.12:67489201::AC 374/1832) Row 10721366 (NC_000004.12:67489201::ACACAC 6/1832)...	-	Apr 26, 2020 (154)
94	Northern Sweden Submission ignored due to conflicting rows: Row 4511775 (NC_000004.11:68354915:AC: 517/600) Row 4511776 (NC_000004.11:68354915::AC 33/600) Row 4511777 (NC_000004.11:68354915::ACAC 28/600)	-	Jul 13, 2019 (153)
95	Northern Sweden Submission ignored due to conflicting rows: Row 4511775 (NC_000004.11:68354915:AC: 517/600) Row 4511776 (NC_000004.11:68354915::AC 33/600) Row 4511777 (NC_000004.11:68354915::ACAC 28/600)	-	Jul 13, 2019 (153)
96	Northern Sweden Submission ignored due to conflicting rows: Row 4511775 (NC_000004.11:68354915:AC: 517/600) Row 4511776 (NC_000004.11:68354915::AC 33/600) Row 4511777 (NC_000004.11:68354915::ACAC 28/600)	-	Jul 13, 2019 (153)
97	8.3KJPN Submission ignored due to conflicting rows: Row 24067850 (NC_000004.11:68354915::AC 3349/16758) Row 24067851 (NC_000004.11:68354915:AC: 5215/16758) Row 24067852 (NC_000004.11:68354915::ACAC 2489/16758)...	-	Apr 26, 2021 (155)
98	8.3KJPN Submission ignored due to conflicting rows: Row 24067850 (NC_000004.11:68354915::AC 3349/16758) Row 24067851 (NC_000004.11:68354915:AC: 5215/16758) Row 24067852 (NC_000004.11:68354915::ACAC 2489/16758)...	-	Apr 26, 2021 (155)
99	8.3KJPN Submission ignored due to conflicting rows: Row 24067850 (NC_000004.11:68354915::AC 3349/16758) Row 24067851 (NC_000004.11:68354915:AC: 5215/16758) Row 24067852 (NC_000004.11:68354915::ACAC 2489/16758)...	-	Apr 26, 2021 (155)
100	8.3KJPN Submission ignored due to conflicting rows: Row 24067850 (NC_000004.11:68354915::AC 3349/16758) Row 24067851 (NC_000004.11:68354915:AC: 5215/16758) Row 24067852 (NC_000004.11:68354915::ACAC 2489/16758)...	-	Apr 26, 2021 (155)
101	8.3KJPN Submission ignored due to conflicting rows: Row 24067850 (NC_000004.11:68354915::AC 3349/16758) Row 24067851 (NC_000004.11:68354915:AC: 5215/16758) Row 24067852 (NC_000004.11:68354915::ACAC 2489/16758)...	-	Apr 26, 2021 (155)
102	8.3KJPN Submission ignored due to conflicting rows: Row 24067850 (NC_000004.11:68354915::AC 3349/16758) Row 24067851 (NC_000004.11:68354915:AC: 5215/16758) Row 24067852 (NC_000004.11:68354915::ACAC 2489/16758)...	-	Apr 26, 2021 (155)
103	14KJPN Submission ignored due to conflicting rows: Row 34385363 (NC_000004.12:67489197::AC 5593/28256) Row 34385364 (NC_000004.12:67489197:AC: 8750/28256) Row 34385365 (NC_000004.12:67489197::ACACAC 93/28256)...	-	Oct 13, 2022 (156)
104	14KJPN Submission ignored due to conflicting rows: Row 34385363 (NC_000004.12:67489197::AC 5593/28256) Row 34385364 (NC_000004.12:67489197:AC: 8750/28256) Row 34385365 (NC_000004.12:67489197::ACACAC 93/28256)...	-	Oct 13, 2022 (156)
105	14KJPN Submission ignored due to conflicting rows: Row 34385363 (NC_000004.12:67489197::AC 5593/28256) Row 34385364 (NC_000004.12:67489197:AC: 8750/28256) Row 34385365 (NC_000004.12:67489197::ACACAC 93/28256)...	-	Oct 13, 2022 (156)
106	14KJPN Submission ignored due to conflicting rows: Row 34385363 (NC_000004.12:67489197::AC 5593/28256) Row 34385364 (NC_000004.12:67489197:AC: 8750/28256) Row 34385365 (NC_000004.12:67489197::ACACAC 93/28256)...	-	Oct 13, 2022 (156)
107	14KJPN Submission ignored due to conflicting rows: Row 34385363 (NC_000004.12:67489197::AC 5593/28256) Row 34385364 (NC_000004.12:67489197:AC: 8750/28256) Row 34385365 (NC_000004.12:67489197::ACACAC 93/28256)...	-	Oct 13, 2022 (156)
108	14KJPN Submission ignored due to conflicting rows: Row 34385363 (NC_000004.12:67489197::AC 5593/28256) Row 34385364 (NC_000004.12:67489197:AC: 8750/28256) Row 34385365 (NC_000004.12:67489197::ACACAC 93/28256)...	-	Oct 13, 2022 (156)
109	UK 10K study - Twins Submission ignored due to conflicting rows: Row 11950024 (NC_000004.11:68354917:AC: 3304/3708) Row 11950025 (NC_000004.11:68354915:ACAC: 178/3708)	-	Apr 26, 2020 (154)
110	UK 10K study - Twins	-	Oct 12, 2018 (152)
111	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 2630394 (NC_000004.11:68354915::AC 37/125) Row 2630395 (NC_000004.11:68354915::ACAC 7/95) Row 2630396 (NC_000004.11:68354915:AC: 80/168)	-	Jul 13, 2019 (153)
112	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 2630394 (NC_000004.11:68354915::AC 37/125) Row 2630395 (NC_000004.11:68354915::ACAC 7/95) Row 2630396 (NC_000004.11:68354915:AC: 80/168)	-	Jul 13, 2019 (153)
113	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 2630394 (NC_000004.11:68354915::AC 37/125) Row 2630395 (NC_000004.11:68354915::ACAC 7/95) Row 2630396 (NC_000004.11:68354915:AC: 80/168)	-	Jul 13, 2019 (153)
114	ALFA	NC_000004.12 - 67489198	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)
rs67881459	Feb 27, 2009 (130)
rs67881460	Feb 27, 2009 (130)
rs71794266	May 11, 2012 (137)
rs72161636	May 11, 2012 (137)
rs147258015	Sep 17, 2011 (135)
rs58666451	May 11, 2012 (137)
rs143908917	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4112794732	NC_000004.12:67489197:ACACACACACAC:	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACA	(self)
2374084651	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACA	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACA	(self)
ss4112794731	NC_000004.12:67489197:ACACACACAC:	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACA	(self)
2374084651	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACA	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACA	(self)
ss4112794730, ss5259509124	NC_000004.12:67489197:ACACACAC:	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACA	(self)
2374084651	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACA	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACA	(self)
ss3712219486, ss4112794729	NC_000004.12:67489197:ACACAC:	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACA	(self)
2374084651	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACA	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACA	(self)
11950025, ss1704192402, ss1704193936, ss2994841884, ss5166098546, ss5844115477	NC_000004.11:68354915:ACAC:	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACA	(self)
ss3954343366, ss4112794728, ss5700548264	NC_000004.12:67489197:ACAC:	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACA	(self)
2374084651	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACA	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACA	(self)
ss3712219485	NC_000004.12:67489199:ACAC:	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACA	(self)
ss79995813, ss80182810	NC_000004.9:68183704:CA:	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss288536096, ss551371672	NC_000004.10:68037510:AC:	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss295169823	NC_000004.10:68037521:CA:	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss295169824	NC_000004.10:68037522:AC:	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss666262221, ss1536411113, ss3731226910, ss3784738270, ss3790193119, ss3795068224, ss3828587158, ss3837733412, ss5166098544, ss5844115476	NC_000004.11:68354915:AC:	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss1710151159, ss1710151189	NC_000004.11:68354917:AC:	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss3064105757, ss3064972676, ss3065954171, ss3647751518, ss3843170290, ss4112794727, ss5259509119, ss5458234946, ss5700548260, ss5863784737	NC_000004.12:67489197:AC:	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
2374084651	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACA	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss3954343363	NC_000004.12:67489199:AC:	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss3712219484	NC_000004.12:67489201:AC:	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss193741894	NT_016354.20:8567839:CA:	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss287749464	NT_022778.16:8565582:AC:	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss95357685	NT_022778.16:8565605:CA:	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss288536098	NC_000004.10:68037535::CA	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
ss3731226911, ss5166098543	NC_000004.11:68354915::AC	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
ss3805042044, ss4112794723, ss5259509121, ss5458234947, ss5700548259	NC_000004.12:67489197::AC	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
2374084651	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACA	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
ss3954343364	NC_000004.12:67489201::AC	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
ss3712219483	NC_000004.12:67489203::AC	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
ss42225639	NT_022778.16:8565582::AC	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
ss288536098	NC_000004.10:68037535::CACA	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACA	(self)
ss3731226912, ss5166098545	NC_000004.11:68354915::ACAC	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACA	(self)
ss4112794724, ss5259509122, ss5458234948, ss5700548262	NC_000004.12:67489197::ACAC	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACA	(self)
2374084651	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACA	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACA	(self)
ss3954343367	NC_000004.12:67489201::ACAC	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACA	(self)
ss3712219482	NC_000004.12:67489203::ACAC	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACA	(self)
ss5166098548	NC_000004.11:68354915::ACACAC	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA	(self)
ss4112794725, ss5259509120, ss5700548261	NC_000004.12:67489197::ACACAC	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA	(self)
2374084651	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA	(self)
ss3954343365	NC_000004.12:67489201::ACACAC	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA	(self)
2374084651	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACA	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACA	(self)
ss3712219481	NC_000004.12:67489203::ACACACAC	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACA	(self)
2374084651	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACA	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACA	(self)
ss5166098547	NC_000004.11:68354915::ACACACACACAC	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACA	(self)
ss4112794726, ss5259509123, ss5700548263	NC_000004.12:67489197::ACACACACACAC	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACA	(self)
2374084651	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACA	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3431351874	NC_000004.12:67489197::ACACACAC	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACA
ss3431351875	NC_000004.12:67489197::ACACACACAC	NC_000004.12:67489197:ACACACACACAC… NC_000004.12:67489197:ACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACA

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

No publications for rs33944071

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

rs33944071