Name: rs112808701
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.

rs112808701

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr15:34574304-34574319 (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)₄ / delTTT / delTT / delT / …
del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dup(T)₁₂
Variation Type: Indel Insertion and Deletion
Frequency: delTT=0.1079 (759/7034, ALFA)
delTTT=0.3243 (1624/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: GOLGA8B : 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	7034	TTTTTTTTTTTTTTTT=0.7523	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0876, TTTTTTTTTTTTTT=0.1079, TTTTTTTTTTTTTTT=0.0506, TTTTTTTTTTTTTTTTT=0.0016, TTTTTTTTTTTTTTTTTT=0.0000	0.805671	0.024953	0.169376	25
European	Sub	6414	TTTTTTTTTTTTTTTT=0.7290	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0957, TTTTTTTTTTTTTT=0.1182, TTTTTTTTTTTTTTT=0.0553, TTTTTTTTTTTTTTTTT=0.0017, TTTTTTTTTTTTTTTTTT=0.0000	0.780582	0.028229	0.191189	18
African	Sub	388	TTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	8	TTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
African American	Sub	380	TTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	26	TTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	18	TTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	8	TTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	18	TTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	72	TTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	18	TTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	98	TTTTTTTTTTTTTTTT=0.96	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.02, TTTTTTTTTTTTTT=0.01, TTTTTTTTTTTTTTT=0.01, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	0.978261	0.0	0.021739	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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	7034	(T)₁₆=0.7523	del(T)₄=0.0000, delTTT=0.0876, delTT=0.1079, delT=0.0506, dupT=0.0016, dupTT=0.0000
Allele Frequency Aggregator	European	Sub	6414	(T)₁₆=0.7290	del(T)₄=0.0000, delTTT=0.0957, delTT=0.1182, delT=0.0553, dupT=0.0017, dupTT=0.0000
Allele Frequency Aggregator	African	Sub	388	(T)₁₆=1.000	del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Other	Sub	98	(T)₁₆=0.96	del(T)₄=0.00, delTTT=0.02, delTT=0.01, delT=0.01, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Latin American 2	Sub	72	(T)₁₆=1.00	del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Asian	Sub	26	(T)₁₆=1.00	del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Latin American 1	Sub	18	(T)₁₆=1.00	del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	South Asian	Sub	18	(T)₁₆=1.00	del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
1000Genomes	Global	Study-wide	5008	(T)₁₆=0.6757	delTTT=0.3243
1000Genomes	African	Sub	1322	(T)₁₆=0.6800	delTTT=0.3200
1000Genomes	East Asian	Sub	1008	(T)₁₆=0.7927	delTTT=0.2073
1000Genomes	Europe	Sub	1006	(T)₁₆=0.7127	delTTT=0.2873
1000Genomes	South Asian	Sub	978	(T)₁₆=0.647	delTTT=0.353
1000Genomes	American	Sub	694	(T)₁₆=0.484	delTTT=0.516

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 15	NC_000015.10:g.34574316_34574319del
GRCh38.p14 chr 15	NC_000015.10:g.34574317_34574319del
GRCh38.p14 chr 15	NC_000015.10:g.34574318_34574319del
GRCh38.p14 chr 15	NC_000015.10:g.34574319del
GRCh38.p14 chr 15	NC_000015.10:g.34574319dup
GRCh38.p14 chr 15	NC_000015.10:g.34574318_34574319dup
GRCh38.p14 chr 15	NC_000015.10:g.34574308_34574319dup
GRCh37.p13 chr 15	NC_000015.9:g.34866517_34866520del
GRCh37.p13 chr 15	NC_000015.9:g.34866518_34866520del
GRCh37.p13 chr 15	NC_000015.9:g.34866519_34866520del
GRCh37.p13 chr 15	NC_000015.9:g.34866520del
GRCh37.p13 chr 15	NC_000015.9:g.34866520dup
GRCh37.p13 chr 15	NC_000015.9:g.34866519_34866520dup
GRCh37.p13 chr 15	NC_000015.9:g.34866509_34866520dup

Gene: GOLGA8B, golgin A8 family member B (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
GOLGA8B transcript variant 1	NM_001023567.5:c.-1123+92… NM_001023567.5:c.-1123+9209_-1123+9212del	N/A	Intron Variant
GOLGA8B transcript variant 2	NR_027410.2:n.	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	(T)₁₆=	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dup(T)₁₂
GRCh38.p14 chr 15	NC_000015.10:g.34574304_34574319=	NC_000015.10:g.34574316_34574319del	NC_000015.10:g.34574317_34574319del	NC_000015.10:g.34574318_34574319del	NC_000015.10:g.34574319del	NC_000015.10:g.34574319dup	NC_000015.10:g.34574318_34574319dup	NC_000015.10:g.34574308_34574319dup
GRCh37.p13 chr 15	NC_000015.9:g.34866505_34866520=	NC_000015.9:g.34866517_34866520del	NC_000015.9:g.34866518_34866520del	NC_000015.9:g.34866519_34866520del	NC_000015.9:g.34866520del	NC_000015.9:g.34866520dup	NC_000015.9:g.34866519_34866520dup	NC_000015.9:g.34866509_34866520dup
GOLGA8B transcript variant 1	NM_001023567.5:c.-1123+9212=	NM_001023567.5:c.-1123+9209_-1123+9212del	NM_001023567.5:c.-1123+9210_-1123+9212del	NM_001023567.5:c.-1123+9211_-1123+9212del	NM_001023567.5:c.-1123+9212del	NM_001023567.5:c.-1123+9212dup	NM_001023567.5:c.-1123+9211_-1123+9212dup	NM_001023567.5:c.-1123+9201_-1123+9212dup
GOLGA8B transcript variant X1	XM_005254389.1:c.-1123+9212=	XM_005254389.1:c.-1123+9209_-1123+9212del	XM_005254389.1:c.-1123+9210_-1123+9212del	XM_005254389.1:c.-1123+9211_-1123+9212del	XM_005254389.1:c.-1123+9212del	XM_005254389.1:c.-1123+9212dup	XM_005254389.1:c.-1123+9211_-1123+9212dup	XM_005254389.1:c.-1123+9201_-1123+9212dup
GOLGA8B transcript variant X2	XM_005254390.1:c.-1123+9212=	XM_005254390.1:c.-1123+9209_-1123+9212del	XM_005254390.1:c.-1123+9210_-1123+9212del	XM_005254390.1:c.-1123+9211_-1123+9212del	XM_005254390.1:c.-1123+9212del	XM_005254390.1:c.-1123+9212dup	XM_005254390.1:c.-1123+9211_-1123+9212dup	XM_005254390.1:c.-1123+9201_-1123+9212dup
GOLGA8B transcript variant X3	XM_005254391.1:c.-1123+9212=	XM_005254391.1:c.-1123+9209_-1123+9212del	XM_005254391.1:c.-1123+9210_-1123+9212del	XM_005254391.1:c.-1123+9211_-1123+9212del	XM_005254391.1:c.-1123+9212del	XM_005254391.1:c.-1123+9212dup	XM_005254391.1:c.-1123+9211_-1123+9212dup	XM_005254391.1:c.-1123+9201_-1123+9212dup

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, 29 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BUSHMAN	ss193377789	Mar 15, 2016 (147)
2	GMI	ss287926009	May 09, 2011 (136)
3	GMI	ss289250648	May 04, 2012 (137)
4	GMI	ss289250649	May 04, 2012 (138)
5	SSMP	ss664265901	Apr 01, 2015 (144)
6	1000GENOMES	ss1374745417	Aug 21, 2014 (142)
7	EVA_UK10K_ALSPAC	ss1708246949	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1708247073	Apr 01, 2015 (144)
9	EVA_UK10K_ALSPAC	ss1710660962	Jan 10, 2018 (151)
10	EVA_UK10K_TWINSUK	ss1710660965	Jan 10, 2018 (151)
11	HAMMER_LAB	ss1808149905	Sep 08, 2015 (146)
12	SYSTEMSBIOZJU	ss2628651023	Nov 08, 2017 (151)
13	SWEGEN	ss3013088206	Nov 08, 2017 (151)
14	URBANLAB	ss3650329582	Oct 12, 2018 (152)
15	EVA_DECODE	ss3697663253	Jul 13, 2019 (153)
16	EVA_DECODE	ss3697663254	Jul 13, 2019 (153)
17	EVA_DECODE	ss3697663255	Jul 13, 2019 (153)
18	EVA_DECODE	ss3697663256	Jul 13, 2019 (153)
19	EVA_DECODE	ss3697663257	Jul 13, 2019 (153)
20	EVA_DECODE	ss3697663258	Jul 13, 2019 (153)
21	ACPOP	ss3740824845	Jul 13, 2019 (153)
22	ACPOP	ss3740824846	Jul 13, 2019 (153)
23	ACPOP	ss3740824847	Jul 13, 2019 (153)
24	PACBIO	ss3787813479	Jul 13, 2019 (153)
25	PACBIO	ss3792831134	Jul 13, 2019 (153)
26	PACBIO	ss3797715609	Jul 13, 2019 (153)
27	KHV_HUMAN_GENOMES	ss3818257143	Jul 13, 2019 (153)
28	EVA	ss3834176973	Apr 27, 2020 (154)
29	EVA	ss3840686370	Apr 27, 2020 (154)
30	EVA	ss3846174662	Apr 27, 2020 (154)
31	KOGIC	ss3975900394	Apr 27, 2020 (154)
32	KOGIC	ss3975900395	Apr 27, 2020 (154)
33	KOGIC	ss3975900396	Apr 27, 2020 (154)
34	KOGIC	ss3975900397	Apr 27, 2020 (154)
35	GNOMAD	ss4286659705	Apr 26, 2021 (155)
36	GNOMAD	ss4286659706	Apr 26, 2021 (155)
37	GNOMAD	ss4286659707	Apr 26, 2021 (155)
38	GNOMAD	ss4286659708	Apr 26, 2021 (155)
39	GNOMAD	ss4286659709	Apr 26, 2021 (155)
40	GNOMAD	ss4286659710	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5215635918	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5215635919	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5215635920	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5215635921	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5215635922	Apr 26, 2021 (155)
46	1000G_HIGH_COVERAGE	ss5298023564	Oct 16, 2022 (156)
47	1000G_HIGH_COVERAGE	ss5298023565	Oct 16, 2022 (156)
48	1000G_HIGH_COVERAGE	ss5298023566	Oct 16, 2022 (156)
49	HUGCELL_USP	ss5491797746	Oct 16, 2022 (156)
50	HUGCELL_USP	ss5491797747	Oct 16, 2022 (156)
51	HUGCELL_USP	ss5491797748	Oct 16, 2022 (156)
52	HUGCELL_USP	ss5491797749	Oct 16, 2022 (156)
53	HUGCELL_USP	ss5491797750	Oct 16, 2022 (156)
54	TOMMO_GENOMICS	ss5769274716	Oct 16, 2022 (156)
55	TOMMO_GENOMICS	ss5769274717	Oct 16, 2022 (156)
56	TOMMO_GENOMICS	ss5769274718	Oct 16, 2022 (156)
57	TOMMO_GENOMICS	ss5769274719	Oct 16, 2022 (156)
58	TOMMO_GENOMICS	ss5769274720	Oct 16, 2022 (156)
59	EVA	ss5828043227	Oct 16, 2022 (156)
60	EVA	ss5828043228	Oct 16, 2022 (156)
61	1000Genomes	NC_000015.9 - 34866505	Oct 12, 2018 (152)
62	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 36659085 (NC_000015.9:34866505:T: 1273/3854) Row 36659086 (NC_000015.9:34866504:TTT: 564/3854)	-	Oct 12, 2018 (152)
63	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 36659085 (NC_000015.9:34866505:T: 1273/3854) Row 36659086 (NC_000015.9:34866504:TTT: 564/3854)	-	Oct 12, 2018 (152)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 465528479 (NC_000015.10:34574303::T 935/133028) Row 465528480 (NC_000015.10:34574303::TT 5/133046) Row 465528481 (NC_000015.10:34574303:T: 24329/132798)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 465528479 (NC_000015.10:34574303::T 935/133028) Row 465528480 (NC_000015.10:34574303::TT 5/133046) Row 465528481 (NC_000015.10:34574303:T: 24329/132798)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 465528479 (NC_000015.10:34574303::T 935/133028) Row 465528480 (NC_000015.10:34574303::TT 5/133046) Row 465528481 (NC_000015.10:34574303:T: 24329/132798)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 465528479 (NC_000015.10:34574303::T 935/133028) Row 465528480 (NC_000015.10:34574303::TT 5/133046) Row 465528481 (NC_000015.10:34574303:T: 24329/132798)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 465528479 (NC_000015.10:34574303::T 935/133028) Row 465528480 (NC_000015.10:34574303::TT 5/133046) Row 465528481 (NC_000015.10:34574303:T: 24329/132798)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 465528479 (NC_000015.10:34574303::T 935/133028) Row 465528480 (NC_000015.10:34574303::TT 5/133046) Row 465528481 (NC_000015.10:34574303:T: 24329/132798)...	-	Apr 26, 2021 (155)
70	Korean Genome Project Submission ignored due to conflicting rows: Row 32278395 (NC_000015.10:34574303:TTT: 273/1832) Row 32278396 (NC_000015.10:34574305:T: 479/1832) Row 32278397 (NC_000015.10:34574304:TT: 140/1832)...	-	Apr 27, 2020 (154)
71	Korean Genome Project Submission ignored due to conflicting rows: Row 32278395 (NC_000015.10:34574303:TTT: 273/1832) Row 32278396 (NC_000015.10:34574305:T: 479/1832) Row 32278397 (NC_000015.10:34574304:TT: 140/1832)...	-	Apr 27, 2020 (154)
72	Korean Genome Project Submission ignored due to conflicting rows: Row 32278395 (NC_000015.10:34574303:TTT: 273/1832) Row 32278396 (NC_000015.10:34574305:T: 479/1832) Row 32278397 (NC_000015.10:34574304:TT: 140/1832)...	-	Apr 27, 2020 (154)
73	Korean Genome Project Submission ignored due to conflicting rows: Row 32278395 (NC_000015.10:34574303:TTT: 273/1832) Row 32278396 (NC_000015.10:34574305:T: 479/1832) Row 32278397 (NC_000015.10:34574304:TT: 140/1832)...	-	Apr 27, 2020 (154)
74	Northern Sweden Submission ignored due to conflicting rows: Row 14109710 (NC_000015.9:34866504:TTT: 82/590) Row 14109711 (NC_000015.9:34866504:TT: 108/590) Row 14109712 (NC_000015.9:34866504:T: 55/590)	-	Jul 13, 2019 (153)
75	Northern Sweden Submission ignored due to conflicting rows: Row 14109710 (NC_000015.9:34866504:TTT: 82/590) Row 14109711 (NC_000015.9:34866504:TT: 108/590) Row 14109712 (NC_000015.9:34866504:T: 55/590)	-	Jul 13, 2019 (153)
76	Northern Sweden Submission ignored due to conflicting rows: Row 14109710 (NC_000015.9:34866504:TTT: 82/590) Row 14109711 (NC_000015.9:34866504:TT: 108/590) Row 14109712 (NC_000015.9:34866504:T: 55/590)	-	Jul 13, 2019 (153)
77	8.3KJPN Submission ignored due to conflicting rows: Row 73605225 (NC_000015.9:34866504:TTT: 2413/16760) Row 73605226 (NC_000015.9:34866504:T: 4281/16760) Row 73605227 (NC_000015.9:34866504:TT: 1103/16760)...	-	Apr 26, 2021 (155)
78	8.3KJPN Submission ignored due to conflicting rows: Row 73605225 (NC_000015.9:34866504:TTT: 2413/16760) Row 73605226 (NC_000015.9:34866504:T: 4281/16760) Row 73605227 (NC_000015.9:34866504:TT: 1103/16760)...	-	Apr 26, 2021 (155)
79	8.3KJPN Submission ignored due to conflicting rows: Row 73605225 (NC_000015.9:34866504:TTT: 2413/16760) Row 73605226 (NC_000015.9:34866504:T: 4281/16760) Row 73605227 (NC_000015.9:34866504:TT: 1103/16760)...	-	Apr 26, 2021 (155)
80	8.3KJPN Submission ignored due to conflicting rows: Row 73605225 (NC_000015.9:34866504:TTT: 2413/16760) Row 73605226 (NC_000015.9:34866504:T: 4281/16760) Row 73605227 (NC_000015.9:34866504:TT: 1103/16760)...	-	Apr 26, 2021 (155)
81	8.3KJPN Submission ignored due to conflicting rows: Row 73605225 (NC_000015.9:34866504:TTT: 2413/16760) Row 73605226 (NC_000015.9:34866504:T: 4281/16760) Row 73605227 (NC_000015.9:34866504:TT: 1103/16760)...	-	Apr 26, 2021 (155)
82	14KJPN Submission ignored due to conflicting rows: Row 103111820 (NC_000015.10:34574303:TTT: 4092/28258) Row 103111821 (NC_000015.10:34574303:T: 7147/28258) Row 103111822 (NC_000015.10:34574303:TT: 1866/28258)...	-	Oct 16, 2022 (156)
83	14KJPN Submission ignored due to conflicting rows: Row 103111820 (NC_000015.10:34574303:TTT: 4092/28258) Row 103111821 (NC_000015.10:34574303:T: 7147/28258) Row 103111822 (NC_000015.10:34574303:TT: 1866/28258)...	-	Oct 16, 2022 (156)
84	14KJPN Submission ignored due to conflicting rows: Row 103111820 (NC_000015.10:34574303:TTT: 4092/28258) Row 103111821 (NC_000015.10:34574303:T: 7147/28258) Row 103111822 (NC_000015.10:34574303:TT: 1866/28258)...	-	Oct 16, 2022 (156)
85	14KJPN Submission ignored due to conflicting rows: Row 103111820 (NC_000015.10:34574303:TTT: 4092/28258) Row 103111821 (NC_000015.10:34574303:T: 7147/28258) Row 103111822 (NC_000015.10:34574303:TT: 1866/28258)...	-	Oct 16, 2022 (156)
86	14KJPN Submission ignored due to conflicting rows: Row 103111820 (NC_000015.10:34574303:TTT: 4092/28258) Row 103111821 (NC_000015.10:34574303:T: 7147/28258) Row 103111822 (NC_000015.10:34574303:TT: 1866/28258)...	-	Oct 16, 2022 (156)
87	UK 10K study - Twins Submission ignored due to conflicting rows: Row 36659085 (NC_000015.9:34866505:T: 1233/3708) Row 36659086 (NC_000015.9:34866504:TTT: 586/3708)	-	Oct 12, 2018 (152)
88	UK 10K study - Twins Submission ignored due to conflicting rows: Row 36659085 (NC_000015.9:34866505:T: 1233/3708) Row 36659086 (NC_000015.9:34866504:TTT: 586/3708)	-	Oct 12, 2018 (152)
89	ALFA	NC_000015.10 - 34574304	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)
rs869227259	Jul 19, 2016 (147)
rs140421838	Oct 19, 2011 (136)
rs200366255	Apr 25, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5215635921	NC_000015.9:34866504:TTTT:	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3697663253, ss4286659710, ss5491797750, ss5769274719	NC_000015.10:34574303:TTTT:	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
1793168700	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss289250649	NC_000015.8:32653796:TTT:	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
66039983, ss1374745417, ss1708246949, ss1708247073, ss1808149905, ss3013088206, ss3740824845, ss5215635918, ss5828043228	NC_000015.9:34866504:TTT:	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3818257143, ss3975900394, ss4286659709, ss5298023564, ss5491797748, ss5769274716	NC_000015.10:34574303:TTT:	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
1793168700	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3697663254	NC_000015.10:34574304:TTT:	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss287926009	NT_010194.17:5657061:TTT:	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3740824846, ss5215635920, ss5828043227	NC_000015.9:34866504:TT:	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss1710660962, ss1710660965	NC_000015.9:34866505:TT:	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4286659708, ss5298023565, ss5491797749, ss5769274718	NC_000015.10:34574303:TT:	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
1793168700	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3975900396	NC_000015.10:34574304:TT:	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3697663255	NC_000015.10:34574305:TT:	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss289250648	NC_000015.8:32653796:T:	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss664265901, ss2628651023, ss3740824847, ss3787813479, ss3792831134, ss3797715609, ss3834176973, ss3840686370, ss5215635919	NC_000015.9:34866504:T:	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
	NC_000015.9:34866505:T:	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3650329582, ss3846174662, ss4286659707, ss5298023566, ss5491797746, ss5769274717	NC_000015.10:34574303:T:	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
1793168700	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3975900395	NC_000015.10:34574305:T:	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3697663256	NC_000015.10:34574306:T:	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss193377789	NT_010194.17:5657061:T:	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss5215635922	NC_000015.9:34866504::T	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4286659705, ss5491797747, ss5769274720	NC_000015.10:34574303::T	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
1793168700	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3975900397	NC_000015.10:34574306::T	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3697663257	NC_000015.10:34574307::T	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4286659706	NC_000015.10:34574303::TT	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
1793168700	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3697663258	NC_000015.10:34574307::TTTTTTTTTTTT	NC_000015.10:34574303:TTTTTTTTTTTT… NC_000015.10:34574303:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs112808701

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

rs112808701