Name: rs35750076
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.

rs35750076

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr8:11344097-11344116 (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)₆ / del(T)₄ / delTTT / delTT…
del(T)₆ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₁₀
Variation Type: Indel Insertion and Deletion
Frequency: delTT=0.2025 (1502/7416, ALFA)
(T)₂₀=0.4681 (2344/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TDH : 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	7416	TTTTTTTTTTTTTTTTTTTT=0.7621	TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.2025, TTTTTTTTTTTTTTTTTTTTT=0.0113, TTTTTTTTTTTTTTTTTTT=0.0240, TTTTTTTTTTTTTTTTTTTTTT=0.0000	0.678664	0.082925	0.238411	32
European	Sub	6320	TTTTTTTTTTTTTTTTTTTT=0.7215	TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.2370, TTTTTTTTTTTTTTTTTTTTT=0.0133, TTTTTTTTTTTTTTTTTTT=0.0282, TTTTTTTTTTTTTTTTTTTTTT=0.0000	0.619487	0.09812	0.282393	32
African	Sub	880	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	42	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	838	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	0	TTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
East Asian	Sub	0	TTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Other Asian	Sub	0	TTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	28	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	50	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	24	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	114	TTTTTTTTTTTTTTTTTTTT=0.965	TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.035, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	0.947368	0.017544	0.035088	8

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	7416	(T)₂₀=0.7621	del(T)₆=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.2025, delT=0.0240, dupT=0.0113, dupTT=0.0000
Allele Frequency Aggregator	European	Sub	6320	(T)₂₀=0.7215	del(T)₆=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.2370, delT=0.0282, dupT=0.0133, dupTT=0.0000
Allele Frequency Aggregator	African	Sub	880	(T)₂₀=1.000	del(T)₆=0.000, 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	114	(T)₂₀=0.965	del(T)₆=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.035, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Latin American 2	Sub	50	(T)₂₀=1.00	del(T)₆=0.00, 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	28	(T)₂₀=1.00	del(T)₆=0.00, 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	24	(T)₂₀=1.00	del(T)₆=0.00, 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	0	(T)₂₀=0	del(T)₆=0, del(T)₄=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0
1000Genomes	Global	Study-wide	5008	(T)₂₀=0.4681	delTT=0.5319
1000Genomes	African	Sub	1322	(T)₂₀=0.7413	delTT=0.2587
1000Genomes	East Asian	Sub	1008	(T)₂₀=0.1141	delTT=0.8859
1000Genomes	Europe	Sub	1006	(T)₂₀=0.5099	delTT=0.4901
1000Genomes	South Asian	Sub	978	(T)₂₀=0.467	delTT=0.533
1000Genomes	American	Sub	694	(T)₂₀=0.402	delTT=0.598

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 8	NC_000008.11:g.11344111_11344116del
GRCh38.p14 chr 8	NC_000008.11:g.11344113_11344116del
GRCh38.p14 chr 8	NC_000008.11:g.11344114_11344116del
GRCh38.p14 chr 8	NC_000008.11:g.11344115_11344116del
GRCh38.p14 chr 8	NC_000008.11:g.11344116del
GRCh38.p14 chr 8	NC_000008.11:g.11344116dup
GRCh38.p14 chr 8	NC_000008.11:g.11344115_11344116dup
GRCh38.p14 chr 8	NC_000008.11:g.11344114_11344116dup
GRCh38.p14 chr 8	NC_000008.11:g.11344107_11344116dup
GRCh37.p13 chr 8	NC_000008.10:g.11201620_11201625del
GRCh37.p13 chr 8	NC_000008.10:g.11201622_11201625del
GRCh37.p13 chr 8	NC_000008.10:g.11201623_11201625del
GRCh37.p13 chr 8	NC_000008.10:g.11201624_11201625del
GRCh37.p13 chr 8	NC_000008.10:g.11201625del
GRCh37.p13 chr 8	NC_000008.10:g.11201625dup
GRCh37.p13 chr 8	NC_000008.10:g.11201624_11201625dup
GRCh37.p13 chr 8	NC_000008.10:g.11201623_11201625dup
GRCh37.p13 chr 8	NC_000008.10:g.11201616_11201625dup
GRCh38.p14 chr 8 fix patch HG76_PATCH	NW_018654717.1:g.2002742_2002747del
GRCh38.p14 chr 8 fix patch HG76_PATCH	NW_018654717.1:g.2002744_2002747del
GRCh38.p14 chr 8 fix patch HG76_PATCH	NW_018654717.1:g.2002745_2002747del
GRCh38.p14 chr 8 fix patch HG76_PATCH	NW_018654717.1:g.2002746_2002747del
GRCh38.p14 chr 8 fix patch HG76_PATCH	NW_018654717.1:g.2002747del
GRCh38.p14 chr 8 fix patch HG76_PATCH	NW_018654717.1:g.2002747dup
GRCh38.p14 chr 8 fix patch HG76_PATCH	NW_018654717.1:g.2002746_2002747dup
GRCh38.p14 chr 8 fix patch HG76_PATCH	NW_018654717.1:g.2002745_2002747dup
GRCh38.p14 chr 8 fix patch HG76_PATCH	NW_018654717.1:g.2002738_2002747dup

Gene: TDH, L-threonine dehydrogenase (pseudogene) (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TDH transcript	NR_001578.1: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)₂₀=	del(T)₆	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₁₀
GRCh38.p14 chr 8	NC_000008.11:g.11344097_11344116=	NC_000008.11:g.11344111_11344116del	NC_000008.11:g.11344113_11344116del	NC_000008.11:g.11344114_11344116del	NC_000008.11:g.11344115_11344116del	NC_000008.11:g.11344116del	NC_000008.11:g.11344116dup	NC_000008.11:g.11344115_11344116dup	NC_000008.11:g.11344114_11344116dup	NC_000008.11:g.11344107_11344116dup
GRCh37.p13 chr 8	NC_000008.10:g.11201606_11201625=	NC_000008.10:g.11201620_11201625del	NC_000008.10:g.11201622_11201625del	NC_000008.10:g.11201623_11201625del	NC_000008.10:g.11201624_11201625del	NC_000008.10:g.11201625del	NC_000008.10:g.11201625dup	NC_000008.10:g.11201624_11201625dup	NC_000008.10:g.11201623_11201625dup	NC_000008.10:g.11201616_11201625dup
GRCh38.p14 chr 8 fix patch HG76_PATCH	NW_018654717.1:g.2002728_2002747=	NW_018654717.1:g.2002742_2002747del	NW_018654717.1:g.2002744_2002747del	NW_018654717.1:g.2002745_2002747del	NW_018654717.1:g.2002746_2002747del	NW_018654717.1:g.2002747del	NW_018654717.1:g.2002747dup	NW_018654717.1:g.2002746_2002747dup	NW_018654717.1:g.2002745_2002747dup	NW_018654717.1:g.2002738_2002747dup

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#.

55 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss4259071	Mar 15, 2016 (147)
2	ABI	ss43145611	Mar 15, 2006 (126)
3	ABI	ss43174115	Dec 04, 2013 (138)
4	HUMANGENOME_JCVI	ss98023001	Mar 15, 2016 (147)
5	PJP	ss295369003	May 31, 2013 (138)
6	BILGI_BIOE	ss666427779	Apr 25, 2013 (138)
7	1000GENOMES	ss1367841622	Aug 21, 2014 (142)
8	EVA_UK10K_ALSPAC	ss1705945619	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1705945871	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1710367142	Apr 01, 2015 (144)
11	EVA_UK10K_ALSPAC	ss1710367176	Apr 01, 2015 (144)
12	SWEGEN	ss3002648355	Jan 10, 2018 (151)
13	MCHAISSO	ss3064288892	Jan 10, 2018 (151)
14	MCHAISSO	ss3065173937	Jan 10, 2018 (151)
15	URBANLAB	ss3648844285	Oct 12, 2018 (152)
16	EVA_DECODE	ss3721384106	Jul 13, 2019 (153)
17	EVA_DECODE	ss3721384107	Jul 13, 2019 (153)
18	EVA_DECODE	ss3721384108	Jul 13, 2019 (153)
19	EVA_DECODE	ss3721384109	Jul 13, 2019 (153)
20	EVA_DECODE	ss3721384110	Jul 13, 2019 (153)
21	EVA_DECODE	ss3721384111	Jul 13, 2019 (153)
22	PACBIO	ss3786059367	Jul 13, 2019 (153)
23	PACBIO	ss3791328262	Jul 13, 2019 (153)
24	PACBIO	ss3796209327	Jul 13, 2019 (153)
25	KHV_HUMAN_GENOMES	ss3810764715	Jul 13, 2019 (153)
26	EVA	ss3839008982	Apr 26, 2020 (154)
27	EVA	ss3844468118	Apr 26, 2020 (154)
28	GNOMAD	ss4178908099	Apr 26, 2021 (155)
29	GNOMAD	ss4178908100	Apr 26, 2021 (155)
30	GNOMAD	ss4178908102	Apr 26, 2021 (155)
31	GNOMAD	ss4178908103	Apr 26, 2021 (155)
32	GNOMAD	ss4178908104	Apr 26, 2021 (155)
33	GNOMAD	ss4178908105	Apr 26, 2021 (155)
34	GNOMAD	ss4178908106	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5187248696	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5187248697	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5187248698	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5187248699	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5187248700	Apr 26, 2021 (155)
40	1000G_HIGH_COVERAGE	ss5276014974	Oct 13, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5276014975	Oct 13, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5276014976	Oct 13, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5276014977	Oct 13, 2022 (156)
44	HUGCELL_USP	ss5472705993	Oct 13, 2022 (156)
45	HUGCELL_USP	ss5472705994	Oct 13, 2022 (156)
46	HUGCELL_USP	ss5472705995	Oct 13, 2022 (156)
47	HUGCELL_USP	ss5472705996	Oct 13, 2022 (156)
48	EVA	ss5509241485	Oct 13, 2022 (156)
49	TOMMO_GENOMICS	ss5728755258	Oct 13, 2022 (156)
50	TOMMO_GENOMICS	ss5728755259	Oct 13, 2022 (156)
51	TOMMO_GENOMICS	ss5728755260	Oct 13, 2022 (156)
52	TOMMO_GENOMICS	ss5728755261	Oct 13, 2022 (156)
53	TOMMO_GENOMICS	ss5728755262	Oct 13, 2022 (156)
54	EVA	ss5830098739	Oct 13, 2022 (156)
55	EVA	ss5830098740	Oct 13, 2022 (156)
56	1000Genomes	NC_000008.10 - 11201606	Oct 12, 2018 (152)
57	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 22597587 (NC_000008.10:11201606:T: 2205/3854) Row 22597588 (NC_000008.10:11201605:TTT: 863/3854)	-	Oct 12, 2018 (152)
58	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 22597587 (NC_000008.10:11201606:T: 2205/3854) Row 22597588 (NC_000008.10:11201605:TTT: 863/3854)	-	Oct 12, 2018 (152)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 286701976 (NC_000008.11:11344096::T 1718/126774) Row 286701977 (NC_000008.11:11344096::TT 2/126792) Row 286701979 (NC_000008.11:11344096:T: 14445/126726)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 286701976 (NC_000008.11:11344096::T 1718/126774) Row 286701977 (NC_000008.11:11344096::TT 2/126792) Row 286701979 (NC_000008.11:11344096:T: 14445/126726)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 286701976 (NC_000008.11:11344096::T 1718/126774) Row 286701977 (NC_000008.11:11344096::TT 2/126792) Row 286701979 (NC_000008.11:11344096:T: 14445/126726)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 286701976 (NC_000008.11:11344096::T 1718/126774) Row 286701977 (NC_000008.11:11344096::TT 2/126792) Row 286701979 (NC_000008.11:11344096:T: 14445/126726)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 286701976 (NC_000008.11:11344096::T 1718/126774) Row 286701977 (NC_000008.11:11344096::TT 2/126792) Row 286701979 (NC_000008.11:11344096:T: 14445/126726)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 286701976 (NC_000008.11:11344096::T 1718/126774) Row 286701977 (NC_000008.11:11344096::TT 2/126792) Row 286701979 (NC_000008.11:11344096:T: 14445/126726)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 286701976 (NC_000008.11:11344096::T 1718/126774) Row 286701977 (NC_000008.11:11344096::TT 2/126792) Row 286701979 (NC_000008.11:11344096:T: 14445/126726)...	-	Apr 26, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 45218003 (NC_000008.10:11201605:TT: 11154/16738) Row 45218004 (NC_000008.10:11201605:T: 2198/16738) Row 45218005 (NC_000008.10:11201605::T 580/16738)...	-	Apr 26, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 45218003 (NC_000008.10:11201605:TT: 11154/16738) Row 45218004 (NC_000008.10:11201605:T: 2198/16738) Row 45218005 (NC_000008.10:11201605::T 580/16738)...	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 45218003 (NC_000008.10:11201605:TT: 11154/16738) Row 45218004 (NC_000008.10:11201605:T: 2198/16738) Row 45218005 (NC_000008.10:11201605::T 580/16738)...	-	Apr 26, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 45218003 (NC_000008.10:11201605:TT: 11154/16738) Row 45218004 (NC_000008.10:11201605:T: 2198/16738) Row 45218005 (NC_000008.10:11201605::T 580/16738)...	-	Apr 26, 2021 (155)
70	8.3KJPN Submission ignored due to conflicting rows: Row 45218003 (NC_000008.10:11201605:TT: 11154/16738) Row 45218004 (NC_000008.10:11201605:T: 2198/16738) Row 45218005 (NC_000008.10:11201605::T 580/16738)...	-	Apr 26, 2021 (155)
71	14KJPN Submission ignored due to conflicting rows: Row 62592362 (NC_000008.11:11344096:TT: 18946/28178) Row 62592363 (NC_000008.11:11344096:TTT: 55/28178) Row 62592364 (NC_000008.11:11344096:T: 3696/28178)...	-	Oct 13, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 62592362 (NC_000008.11:11344096:TT: 18946/28178) Row 62592363 (NC_000008.11:11344096:TTT: 55/28178) Row 62592364 (NC_000008.11:11344096:T: 3696/28178)...	-	Oct 13, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 62592362 (NC_000008.11:11344096:TT: 18946/28178) Row 62592363 (NC_000008.11:11344096:TTT: 55/28178) Row 62592364 (NC_000008.11:11344096:T: 3696/28178)...	-	Oct 13, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 62592362 (NC_000008.11:11344096:TT: 18946/28178) Row 62592363 (NC_000008.11:11344096:TTT: 55/28178) Row 62592364 (NC_000008.11:11344096:T: 3696/28178)...	-	Oct 13, 2022 (156)
75	14KJPN Submission ignored due to conflicting rows: Row 62592362 (NC_000008.11:11344096:TT: 18946/28178) Row 62592363 (NC_000008.11:11344096:TTT: 55/28178) Row 62592364 (NC_000008.11:11344096:T: 3696/28178)...	-	Oct 13, 2022 (156)
76	UK 10K study - Twins Submission ignored due to conflicting rows: Row 22597587 (NC_000008.10:11201606:T: 2164/3708) Row 22597588 (NC_000008.10:11201605:TTT: 784/3708)	-	Oct 12, 2018 (152)
77	UK 10K study - Twins Submission ignored due to conflicting rows: Row 22597587 (NC_000008.10:11201606:T: 2164/3708) Row 22597588 (NC_000008.10:11201605:TTT: 784/3708)	-	Oct 12, 2018 (152)
78	ALFA	NC_000008.11 - 11344097	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)
rs35917840	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4178908106	NC_000008.11:11344096:TTTTTT:	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
272691189	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4178908105	NC_000008.11:11344096:TTTT:	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
272691189	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss1705945619, ss1705945871, ss5187248699, ss5830098740	NC_000008.10:11201605:TTT:	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3721384106, ss4178908104, ss5276014977, ss5472705993, ss5728755259	NC_000008.11:11344096:TTT:	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
272691189	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4259071	NT_077531.4:3676973:TTT:	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
40641339, ss666427779, ss1367841622, ss3002648355, ss3786059367, ss3791328262, ss3796209327, ss3839008982, ss5187248696, ss5830098739	NC_000008.10:11201605:TT:	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss1710367142, ss1710367176	NC_000008.10:11201606:TT:	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3064288892, ss3065173937, ss3648844285, ss3810764715, ss3844468118, ss4178908103, ss5276014974, ss5472705994, ss5728755258	NC_000008.11:11344096:TT:	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
272691189	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3721384107	NC_000008.11:11344097:TT:	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss295369003	NC_000008.9:11239034:T:	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss5187248697	NC_000008.10:11201605:T:	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
	NC_000008.10:11201606:T:	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4178908102, ss5276014975, ss5472705995, ss5728755260	NC_000008.11:11344096:T:	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
272691189	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3721384108	NC_000008.11:11344098:T:	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss43145611	NT_077531.4:3676956:T:	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss43174115	NT_077531.4:3676957:T:	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss98023001	NT_077531.4:3676975:T:	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss5187248698	NC_000008.10:11201605::T	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4178908099, ss5276014976, ss5472705996, ss5728755261	NC_000008.11:11344096::T	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
272691189	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3721384109	NC_000008.11:11344099::T	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss98023001	NT_077531.4:3676975:T:TT	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss5187248700, ss5509241485	NC_000008.10:11201605::TT	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4178908100, ss5728755262	NC_000008.11:11344096::TT	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
272691189	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3721384110	NC_000008.11:11344099::TTT	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3721384111	NC_000008.11:11344099::TTTTTTTTTT	NC_000008.11:11344096:TTTTTTTTTTTT… NC_000008.11:11344096:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs35750076

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

rs35750076