Name: rs10608601
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.

rs10608601

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:95392431-95392444 (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(T)₇ / del(T)₆ / del(T)₅ / del(…
del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT
Variation Type: Indel Insertion and Deletion
Frequency: (T)₁₄=0.3830 (1918/5008, 1000G)
del(T)₇=0.0000 (0/4308, ALFA)
del(T)₆=0.0000 (0/4308, ALFA) (+ 7 more)
del(T)₅=0.0000 (0/4308, ALFA)
del(T)₄=0.0000 (0/4308, ALFA)
delTTT=0.0000 (0/4308, ALFA)
delTT=0.0000 (0/4308, ALFA)
delT=0.0000 (0/4308, ALFA)
dupT=0.0000 (0/4308, ALFA)
del(T)₅=0.0846 (326/3854, ALSPAC)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: UNC5C : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

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

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	HWEP
Total	Global	4308	TTTTTTTTTTTTTT=1.0000	TTTTTTT=0.0000, TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000	1.0	N/A
European	Sub	3546	TTTTTTTTTTTTTT=1.0000	TTTTTTT=0.0000, TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	414	TTTTTTTTTTTTTT=1.000	TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	1.0	N/A
African Others	Sub	18	TTTTTTTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	N/A
African American	Sub	396	TTTTTTTTTTTTTT=1.000	TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	1.0	N/A
Asian	Sub	4	TTTTTTTTTTTTTT=1.0	TTTTTTT=0.0, TTTTTTTT=0.0, TTTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0	1.0	N/A
East Asian	Sub	2	TTTTTTTTTTTTTT=1.0	TTTTTTT=0.0, TTTTTTTT=0.0, TTTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0	1.0	N/A
Other Asian	Sub	2	TTTTTTTTTTTTTT=1.0	TTTTTTT=0.0, TTTTTTTT=0.0, TTTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0	1.0	N/A
Latin American 1	Sub	60	TTTTTTTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 2	Sub	112	TTTTTTTTTTTTTT=1.000	TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	28	TTTTTTTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	144	TTTTTTTTTTTTTT=1.000	TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	1.0	N/A

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

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
1000Genomes	Global	Study-wide	5008	(T)₁₄=0.3830	delTT=0.6170
1000Genomes	African	Sub	1322	(T)₁₄=0.3169	delTT=0.6831
1000Genomes	East Asian	Sub	1008	(T)₁₄=0.1260	delTT=0.8740
1000Genomes	Europe	Sub	1006	(T)₁₄=0.6213	delTT=0.3787
1000Genomes	South Asian	Sub	978	(T)₁₄=0.391	delTT=0.609
1000Genomes	American	Sub	694	(T)₁₄=0.526	delTT=0.474
Allele Frequency Aggregator	Total	Global	4308	(T)₁₄=1.0000	del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000
Allele Frequency Aggregator	European	Sub	3546	(T)₁₄=1.0000	del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000
Allele Frequency Aggregator	African	Sub	414	(T)₁₄=1.000	del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000
Allele Frequency Aggregator	Other	Sub	144	(T)₁₄=1.000	del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000
Allele Frequency Aggregator	Latin American 2	Sub	112	(T)₁₄=1.000	del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	60	(T)₁₄=1.00	del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00
Allele Frequency Aggregator	South Asian	Sub	28	(T)₁₄=1.00	del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00
Allele Frequency Aggregator	Asian	Sub	4	(T)₁₄=1.0	del(T)₇=0.0, del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(T)₁₄=0.9154	del(T)₅=0.0846

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.95392438_95392444del
GRCh38.p14 chr 4	NC_000004.12:g.95392439_95392444del
GRCh38.p14 chr 4	NC_000004.12:g.95392440_95392444del
GRCh38.p14 chr 4	NC_000004.12:g.95392441_95392444del
GRCh38.p14 chr 4	NC_000004.12:g.95392442_95392444del
GRCh38.p14 chr 4	NC_000004.12:g.95392443_95392444del
GRCh38.p14 chr 4	NC_000004.12:g.95392444del
GRCh38.p14 chr 4	NC_000004.12:g.95392444dup
GRCh38.p14 chr 4	NC_000004.12:g.95392443_95392444dup
GRCh37.p13 chr 4	NC_000004.11:g.96313589_96313595del
GRCh37.p13 chr 4	NC_000004.11:g.96313590_96313595del
GRCh37.p13 chr 4	NC_000004.11:g.96313591_96313595del
GRCh37.p13 chr 4	NC_000004.11:g.96313592_96313595del
GRCh37.p13 chr 4	NC_000004.11:g.96313593_96313595del
GRCh37.p13 chr 4	NC_000004.11:g.96313594_96313595del
GRCh37.p13 chr 4	NC_000004.11:g.96313595del
GRCh37.p13 chr 4	NC_000004.11:g.96313595dup
GRCh37.p13 chr 4	NC_000004.11:g.96313594_96313595dup

Gene: UNC5C, unc-5 netrin receptor C (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
UNC5C transcript	NM_003728.4:c.125-56806_1… NM_003728.4:c.125-56806_125-56800del	N/A	Intron Variant
UNC5C transcript variant X1	XM_005263321.4:c.125-5680… XM_005263321.4:c.125-56806_125-56800del	N/A	Intron Variant
UNC5C transcript variant X2	XM_047416345.1:c.	N/A	Genic Upstream Transcript Variant
UNC5C transcript variant X3	XM_047416346.1:c.	N/A	Genic Upstream Transcript Variant

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

Not Reported in ClinVar

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

Placement	(T)₁₄=	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT
GRCh38.p14 chr 4	NC_000004.12:g.95392431_95392444=	NC_000004.12:g.95392438_95392444del	NC_000004.12:g.95392439_95392444del	NC_000004.12:g.95392440_95392444del	NC_000004.12:g.95392441_95392444del	NC_000004.12:g.95392442_95392444del	NC_000004.12:g.95392443_95392444del	NC_000004.12:g.95392444del	NC_000004.12:g.95392444dup	NC_000004.12:g.95392443_95392444dup
GRCh37.p13 chr 4	NC_000004.11:g.96313582_96313595=	NC_000004.11:g.96313589_96313595del	NC_000004.11:g.96313590_96313595del	NC_000004.11:g.96313591_96313595del	NC_000004.11:g.96313592_96313595del	NC_000004.11:g.96313593_96313595del	NC_000004.11:g.96313594_96313595del	NC_000004.11:g.96313595del	NC_000004.11:g.96313595dup	NC_000004.11:g.96313594_96313595dup
UNC5C transcript	NM_003728.3:c.125-56800=	NM_003728.3:c.125-56806_125-56800del	NM_003728.3:c.125-56805_125-56800del	NM_003728.3:c.125-56804_125-56800del	NM_003728.3:c.125-56803_125-56800del	NM_003728.3:c.125-56802_125-56800del	NM_003728.3:c.125-56801_125-56800del	NM_003728.3:c.125-56800del	NM_003728.3:c.125-56800dup	NM_003728.3:c.125-56801_125-56800dup
UNC5C transcript	NM_003728.4:c.125-56800=	NM_003728.4:c.125-56806_125-56800del	NM_003728.4:c.125-56805_125-56800del	NM_003728.4:c.125-56804_125-56800del	NM_003728.4:c.125-56803_125-56800del	NM_003728.4:c.125-56802_125-56800del	NM_003728.4:c.125-56801_125-56800del	NM_003728.4:c.125-56800del	NM_003728.4:c.125-56800dup	NM_003728.4:c.125-56801_125-56800dup
UNC5C transcript variant X1	XM_005263321.1:c.125-56800=	XM_005263321.1:c.125-56806_125-56800del	XM_005263321.1:c.125-56805_125-56800del	XM_005263321.1:c.125-56804_125-56800del	XM_005263321.1:c.125-56803_125-56800del	XM_005263321.1:c.125-56802_125-56800del	XM_005263321.1:c.125-56801_125-56800del	XM_005263321.1:c.125-56800del	XM_005263321.1:c.125-56800dup	XM_005263321.1:c.125-56801_125-56800dup
UNC5C transcript variant X1	XM_005263321.4:c.125-56800=	XM_005263321.4:c.125-56806_125-56800del	XM_005263321.4:c.125-56805_125-56800del	XM_005263321.4:c.125-56804_125-56800del	XM_005263321.4:c.125-56803_125-56800del	XM_005263321.4:c.125-56802_125-56800del	XM_005263321.4:c.125-56801_125-56800del	XM_005263321.4:c.125-56800del	XM_005263321.4:c.125-56800dup	XM_005263321.4:c.125-56801_125-56800dup

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#.

58 SubSNP, 30 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	DEVINE_LAB	ss15033539	Mar 15, 2016 (147)
2	HGSV	ss80378833	Aug 21, 2014 (144)
3	HUMANGENOME_JCVI	ss95974455	Feb 05, 2009 (130)
4	GMI	ss288559216	May 04, 2012 (137)
5	GMI	ss288559218	May 04, 2012 (137)
6	PJP	ss295178413	May 09, 2011 (134)
7	PJP	ss295178414	May 09, 2011 (137)
8	1000GENOMES	ss1372504715	Aug 21, 2014 (142)
9	EVA_UK10K_ALSPAC	ss1704268326	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1704268387	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1710159447	Apr 01, 2015 (144)
12	EVA_UK10K_ALSPAC	ss1710159460	Apr 01, 2015 (144)
13	PADH-LAB_SPU	ss1751464826	Sep 08, 2015 (146)
14	EVA_DECODE	ss3712603165	Jul 13, 2019 (153)
15	EVA_DECODE	ss3712603166	Jul 13, 2019 (153)
16	EVA_DECODE	ss3712603167	Jul 13, 2019 (153)
17	EVA_DECODE	ss3712603168	Jul 13, 2019 (153)
18	EVA_DECODE	ss3712603169	Jul 13, 2019 (153)
19	EVA_DECODE	ss3712603170	Jul 13, 2019 (153)
20	ACPOP	ss3731397759	Jul 13, 2019 (153)
21	ACPOP	ss3731397760	Jul 13, 2019 (153)
22	ACPOP	ss3731397761	Jul 13, 2019 (153)
23	PACBIO	ss3784794527	Jul 13, 2019 (153)
24	PACBIO	ss3790240289	Jul 13, 2019 (153)
25	PACBIO	ss3795115677	Jul 13, 2019 (153)
26	KHV_HUMAN_GENOMES	ss3805283111	Jul 13, 2019 (153)
27	KOGIC	ss3954696091	Apr 26, 2020 (154)
28	KOGIC	ss3954696092	Apr 26, 2020 (154)
29	KOGIC	ss3954696093	Apr 26, 2020 (154)
30	KOGIC	ss3954696094	Apr 26, 2020 (154)
31	GNOMAD	ss4116250520	Apr 26, 2021 (155)
32	GNOMAD	ss4116250522	Apr 26, 2021 (155)
33	GNOMAD	ss4116250523	Apr 26, 2021 (155)
34	GNOMAD	ss4116250524	Apr 26, 2021 (155)
35	GNOMAD	ss4116250525	Apr 26, 2021 (155)
36	GNOMAD	ss4116250526	Apr 26, 2021 (155)
37	GNOMAD	ss4116250527	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5166964711	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5166964712	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5166964713	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5166964714	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5166964715	Apr 26, 2021 (155)
43	1000G_HIGH_COVERAGE	ss5260194929	Oct 17, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5260194930	Oct 17, 2022 (156)
45	1000G_HIGH_COVERAGE	ss5260194931	Oct 17, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5260194932	Oct 17, 2022 (156)
47	1000G_HIGH_COVERAGE	ss5260194933	Oct 17, 2022 (156)
48	HUGCELL_USP	ss5458847599	Oct 17, 2022 (156)
49	HUGCELL_USP	ss5458847600	Oct 17, 2022 (156)
50	HUGCELL_USP	ss5458847601	Oct 17, 2022 (156)
51	HUGCELL_USP	ss5458847602	Oct 17, 2022 (156)
52	HUGCELL_USP	ss5458847603	Oct 17, 2022 (156)
53	TOMMO_GENOMICS	ss5701663338	Oct 17, 2022 (156)
54	TOMMO_GENOMICS	ss5701663339	Oct 17, 2022 (156)
55	TOMMO_GENOMICS	ss5701663340	Oct 17, 2022 (156)
56	TOMMO_GENOMICS	ss5701663341	Oct 17, 2022 (156)
57	TOMMO_GENOMICS	ss5701663342	Oct 17, 2022 (156)
58	EVA	ss5864571622	Oct 17, 2022 (156)
59	1000Genomes	NC_000004.11 - 96313582	Oct 12, 2018 (152)
60	The Avon Longitudinal Study of Parents and Children	NC_000004.11 - 96313582	Oct 12, 2018 (152)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 158034407 (NC_000004.12:95392430::T 20/100468) Row 158034409 (NC_000004.12:95392430:T: 2431/100404) Row 158034410 (NC_000004.12:95392430:TT: 28944/100246)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 158034407 (NC_000004.12:95392430::T 20/100468) Row 158034409 (NC_000004.12:95392430:T: 2431/100404) Row 158034410 (NC_000004.12:95392430:TT: 28944/100246)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 158034407 (NC_000004.12:95392430::T 20/100468) Row 158034409 (NC_000004.12:95392430:T: 2431/100404) Row 158034410 (NC_000004.12:95392430:TT: 28944/100246)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 158034407 (NC_000004.12:95392430::T 20/100468) Row 158034409 (NC_000004.12:95392430:T: 2431/100404) Row 158034410 (NC_000004.12:95392430:TT: 28944/100246)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 158034407 (NC_000004.12:95392430::T 20/100468) Row 158034409 (NC_000004.12:95392430:T: 2431/100404) Row 158034410 (NC_000004.12:95392430:TT: 28944/100246)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 158034407 (NC_000004.12:95392430::T 20/100468) Row 158034409 (NC_000004.12:95392430:T: 2431/100404) Row 158034410 (NC_000004.12:95392430:TT: 28944/100246)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 158034407 (NC_000004.12:95392430::T 20/100468) Row 158034409 (NC_000004.12:95392430:T: 2431/100404) Row 158034410 (NC_000004.12:95392430:TT: 28944/100246)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 158034407 (NC_000004.12:95392430::T 20/100468) Row 158034409 (NC_000004.12:95392430:T: 2431/100404) Row 158034410 (NC_000004.12:95392430:TT: 28944/100246)...	-	Apr 26, 2021 (155)
69	Korean Genome Project Submission ignored due to conflicting rows: Row 11074092 (NC_000004.12:95392435:TT: 1131/1832) Row 11074093 (NC_000004.12:95392431:TTTTTT: 245/1832) Row 11074094 (NC_000004.12:95392432:TTTTT: 175/1832)...	-	Apr 26, 2020 (154)
70	Korean Genome Project Submission ignored due to conflicting rows: Row 11074092 (NC_000004.12:95392435:TT: 1131/1832) Row 11074093 (NC_000004.12:95392431:TTTTTT: 245/1832) Row 11074094 (NC_000004.12:95392432:TTTTT: 175/1832)...	-	Apr 26, 2020 (154)
71	Korean Genome Project Submission ignored due to conflicting rows: Row 11074092 (NC_000004.12:95392435:TT: 1131/1832) Row 11074093 (NC_000004.12:95392431:TTTTTT: 245/1832) Row 11074094 (NC_000004.12:95392432:TTTTT: 175/1832)...	-	Apr 26, 2020 (154)
72	Korean Genome Project Submission ignored due to conflicting rows: Row 11074092 (NC_000004.12:95392435:TT: 1131/1832) Row 11074093 (NC_000004.12:95392431:TTTTTT: 245/1832) Row 11074094 (NC_000004.12:95392432:TTTTT: 175/1832)...	-	Apr 26, 2020 (154)
73	Northern Sweden Submission ignored due to conflicting rows: Row 4682624 (NC_000004.11:96313581:TT: 136/552) Row 4682625 (NC_000004.11:96313581:T: 9/552) Row 4682626 (NC_000004.11:96313581:TTTTT: 67/552)	-	Jul 13, 2019 (153)
74	Northern Sweden Submission ignored due to conflicting rows: Row 4682624 (NC_000004.11:96313581:TT: 136/552) Row 4682625 (NC_000004.11:96313581:T: 9/552) Row 4682626 (NC_000004.11:96313581:TTTTT: 67/552)	-	Jul 13, 2019 (153)
75	Northern Sweden Submission ignored due to conflicting rows: Row 4682624 (NC_000004.11:96313581:TT: 136/552) Row 4682625 (NC_000004.11:96313581:T: 9/552) Row 4682626 (NC_000004.11:96313581:TTTTT: 67/552)	-	Jul 13, 2019 (153)
76	8.3KJPN Submission ignored due to conflicting rows: Row 24934018 (NC_000004.11:96313581:TT: 10897/16760) Row 24934019 (NC_000004.11:96313581:TTTTTT: 1853/16760) Row 24934020 (NC_000004.11:96313581:TTTTT: 1519/16760)...	-	Apr 26, 2021 (155)
77	8.3KJPN Submission ignored due to conflicting rows: Row 24934018 (NC_000004.11:96313581:TT: 10897/16760) Row 24934019 (NC_000004.11:96313581:TTTTTT: 1853/16760) Row 24934020 (NC_000004.11:96313581:TTTTT: 1519/16760)...	-	Apr 26, 2021 (155)
78	8.3KJPN Submission ignored due to conflicting rows: Row 24934018 (NC_000004.11:96313581:TT: 10897/16760) Row 24934019 (NC_000004.11:96313581:TTTTTT: 1853/16760) Row 24934020 (NC_000004.11:96313581:TTTTT: 1519/16760)...	-	Apr 26, 2021 (155)
79	8.3KJPN Submission ignored due to conflicting rows: Row 24934018 (NC_000004.11:96313581:TT: 10897/16760) Row 24934019 (NC_000004.11:96313581:TTTTTT: 1853/16760) Row 24934020 (NC_000004.11:96313581:TTTTT: 1519/16760)...	-	Apr 26, 2021 (155)
80	8.3KJPN Submission ignored due to conflicting rows: Row 24934018 (NC_000004.11:96313581:TT: 10897/16760) Row 24934019 (NC_000004.11:96313581:TTTTTT: 1853/16760) Row 24934020 (NC_000004.11:96313581:TTTTT: 1519/16760)...	-	Apr 26, 2021 (155)
81	14KJPN Submission ignored due to conflicting rows: Row 35500442 (NC_000004.12:95392430:TTTTTT: 3116/28258) Row 35500443 (NC_000004.12:95392430:TT: 18377/28258) Row 35500444 (NC_000004.12:95392430:TTTTT: 2582/28258)...	-	Oct 17, 2022 (156)
82	14KJPN Submission ignored due to conflicting rows: Row 35500442 (NC_000004.12:95392430:TTTTTT: 3116/28258) Row 35500443 (NC_000004.12:95392430:TT: 18377/28258) Row 35500444 (NC_000004.12:95392430:TTTTT: 2582/28258)...	-	Oct 17, 2022 (156)
83	14KJPN Submission ignored due to conflicting rows: Row 35500442 (NC_000004.12:95392430:TTTTTT: 3116/28258) Row 35500443 (NC_000004.12:95392430:TT: 18377/28258) Row 35500444 (NC_000004.12:95392430:TTTTT: 2582/28258)...	-	Oct 17, 2022 (156)
84	14KJPN Submission ignored due to conflicting rows: Row 35500442 (NC_000004.12:95392430:TTTTTT: 3116/28258) Row 35500443 (NC_000004.12:95392430:TT: 18377/28258) Row 35500444 (NC_000004.12:95392430:TTTTT: 2582/28258)...	-	Oct 17, 2022 (156)
85	14KJPN Submission ignored due to conflicting rows: Row 35500442 (NC_000004.12:95392430:TTTTTT: 3116/28258) Row 35500443 (NC_000004.12:95392430:TT: 18377/28258) Row 35500444 (NC_000004.12:95392430:TTTTT: 2582/28258)...	-	Oct 17, 2022 (156)
86	UK 10K study - Twins Submission ignored due to conflicting rows: Row 12408019 (NC_000004.11:96313584:TT: 1279/3708) Row 12408020 (NC_000004.11:96313581:TTTTT: 333/3708)	-	Apr 26, 2020 (154)
87	UK 10K study - Twins	-	Oct 12, 2018 (152)
88	ALFA	NC_000004.12 - 95392431	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)
rs67355914	Feb 27, 2009 (130)
rs147155150	May 11, 2012 (137)
rs570067497	Jul 01, 2015 (144)
rs33952391	May 23, 2006 (127)
rs61708054	May 27, 2008 (130)
rs67384673	Jul 30, 2012 (137)
rs67384674	Feb 27, 2009 (130)
rs72140084	Oct 16, 2011 (136)
rs201519028	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5166964715	NC_000004.11:96313581:TTTTTTT:	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTT	(self)
ss3954696094, ss4116250527, ss5701663342	NC_000004.12:95392430:TTTTTTT:	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTT	(self)
7012592646	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTT	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTT	(self)
ss5166964712	NC_000004.11:96313581:TTTTTT:	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTT	(self)
ss1751464826	NC_000004.11:96313589:TTTTTT:	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTT	(self)
ss4116250526, ss5260194932, ss5458847600, ss5701663338	NC_000004.12:95392430:TTTTTT:	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTT	(self)
7012592646	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTT	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTT	(self)
ss3954696092	NC_000004.12:95392431:TTTTTT:	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTT	(self)
12408020, ss1704268326, ss1704268387, ss3731397761, ss3784794527, ss5166964713	NC_000004.11:96313581:TTTTT:	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss3712603165, ss4116250525, ss5260194930, ss5458847601, ss5701663340	NC_000004.12:95392430:TTTTT:	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTT	(self)
7012592646	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTT	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss3954696093	NC_000004.12:95392432:TTTTT:	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss5166964714	NC_000004.11:96313581:TTTT:	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4116250524, ss5260194931, ss5458847603, ss5701663341	NC_000004.12:95392430:TTTT:	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTTT	(self)
7012592646	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTTT	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss3712603166	NC_000004.12:95392431:TTTT:	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4116250523	NC_000004.12:95392430:TTT:	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
7012592646	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3712603167	NC_000004.12:95392432:TTT:	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss80378833	NC_000004.9:96670771:TT:	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss288559218, ss295178413	NC_000004.10:96532604:TT:	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss295178414	NC_000004.10:96532616:TT:	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
22310926, ss1372504715, ss3731397759, ss5166964711	NC_000004.11:96313581:TT:	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss1710159447, ss1710159460	NC_000004.11:96313584:TT:	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3805283111, ss4116250522, ss5260194929, ss5458847599, ss5701663339	NC_000004.12:95392430:TT:	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
7012592646	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3712603168	NC_000004.12:95392433:TT:	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3954696091	NC_000004.12:95392435:TT:	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss15033539	NT_016354.19:20861314:TT:	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss288559216	NC_000004.10:96532604:T:	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3731397760, ss3790240289, ss3795115677	NC_000004.11:96313581:T:	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss5260194933, ss5458847602, ss5864571622	NC_000004.12:95392430:T:	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
7012592646	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3712603169	NC_000004.12:95392434:T:	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4116250520	NC_000004.12:95392430::T	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
7012592646	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3712603170	NC_000004.12:95392435::T	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss95974455	NT_016354.19:20861315:T:TTT	NC_000004.12:95392430:TTTTTTTTTTTT… NC_000004.12:95392430:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(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 rs10608601

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

rs10608601