Name: rs756133661
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.

rs756133661

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr9:128413077-128413096 (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)₁₂ / del(T)₇ / del(T)₅ / del…
del(T)₁₂ / del(T)₇ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₁₂=0.000004 (1/264690, TOPMED)
delT=0.02247 (263/11704, ALFA)
delT=0.35 (14/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: None
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	11704	TTTTTTTTTTTTTTTTTTTT=0.96232	TTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.01324, TTTTTTTTTTTTTTTTTTT=0.02247, TTTTTTTTTTTTTTTTTTTTT=0.00197, TTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTT=0.00000	0.958311	0.002287	0.039402	22
European	Sub	9750	TTTTTTTTTTTTTTTTTTTT=0.9549	TTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0158, TTTTTTTTTTTTTTTTTTT=0.0270, TTTTTTTTTTTTTTTTTTTTT=0.0024, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.949671	0.002761	0.047568	16
African	Sub	1122	TTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	30	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1092	TTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	42	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	32	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	10	TTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	98	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	400	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	52	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	240	TTTTTTTTTTTTTTTTTTTT=0.996	TTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.004, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	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
TopMed	Global	Study-wide	264690	(T)₂₀=0.999996	del(T)₁₂=0.000004
Allele Frequency Aggregator	Total	Global	11704	(T)₂₀=0.96232	del(T)₁₂=0.00000, del(T)₇=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.01324, delT=0.02247, dupT=0.00197, dupTT=0.00000, dupTTT=0.00000
Allele Frequency Aggregator	European	Sub	9750	(T)₂₀=0.9549	del(T)₁₂=0.0000, del(T)₇=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0158, delT=0.0270, dupT=0.0024, dupTT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator	African	Sub	1122	(T)₂₀=1.0000	del(T)₁₂=0.0000, del(T)₇=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	400	(T)₂₀=1.000	del(T)₁₂=0.000, del(T)₇=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Other	Sub	240	(T)₂₀=0.996	del(T)₁₂=0.000, del(T)₇=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.004, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	98	(T)₂₀=1.00	del(T)₁₂=0.00, del(T)₇=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	South Asian	Sub	52	(T)₂₀=1.00	del(T)₁₂=0.00, del(T)₇=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	Asian	Sub	42	(T)₂₀=1.00	del(T)₁₂=0.00, del(T)₇=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
The Danish reference pan genome	Danish	Study-wide	40	(T)₂₀=0.65	delT=0.35

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 9	NC_000009.12:g.128413085_128413096del
GRCh38.p14 chr 9	NC_000009.12:g.128413090_128413096del
GRCh38.p14 chr 9	NC_000009.12:g.128413092_128413096del
GRCh38.p14 chr 9	NC_000009.12:g.128413093_128413096del
GRCh38.p14 chr 9	NC_000009.12:g.128413094_128413096del
GRCh38.p14 chr 9	NC_000009.12:g.128413095_128413096del
GRCh38.p14 chr 9	NC_000009.12:g.128413096del
GRCh38.p14 chr 9	NC_000009.12:g.128413096dup
GRCh38.p14 chr 9	NC_000009.12:g.128413095_128413096dup
GRCh38.p14 chr 9	NC_000009.12:g.128413094_128413096dup
GRCh38.p14 chr 9	NC_000009.12:g.128413093_128413096dup
GRCh38.p14 chr 9	NC_000009.12:g.128413092_128413096dup
GRCh38.p14 chr 9	NC_000009.12:g.128413091_128413096dup
GRCh37.p13 chr 9	NC_000009.11:g.131175364_131175375del
GRCh37.p13 chr 9	NC_000009.11:g.131175369_131175375del
GRCh37.p13 chr 9	NC_000009.11:g.131175371_131175375del
GRCh37.p13 chr 9	NC_000009.11:g.131175372_131175375del
GRCh37.p13 chr 9	NC_000009.11:g.131175373_131175375del
GRCh37.p13 chr 9	NC_000009.11:g.131175374_131175375del
GRCh37.p13 chr 9	NC_000009.11:g.131175375del
GRCh37.p13 chr 9	NC_000009.11:g.131175375dup
GRCh37.p13 chr 9	NC_000009.11:g.131175374_131175375dup
GRCh37.p13 chr 9	NC_000009.11:g.131175373_131175375dup
GRCh37.p13 chr 9	NC_000009.11:g.131175372_131175375dup
GRCh37.p13 chr 9	NC_000009.11:g.131175371_131175375dup
GRCh37.p13 chr 9	NC_000009.11:g.131175370_131175375dup

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)₁₂	del(T)₇	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆
GRCh38.p14 chr 9	NC_000009.12:g.128413077_128413096=	NC_000009.12:g.128413085_128413096del	NC_000009.12:g.128413090_128413096del	NC_000009.12:g.128413092_128413096del	NC_000009.12:g.128413093_128413096del	NC_000009.12:g.128413094_128413096del	NC_000009.12:g.128413095_128413096del	NC_000009.12:g.128413096del	NC_000009.12:g.128413096dup	NC_000009.12:g.128413095_128413096dup	NC_000009.12:g.128413094_128413096dup	NC_000009.12:g.128413093_128413096dup	NC_000009.12:g.128413092_128413096dup	NC_000009.12:g.128413091_128413096dup
GRCh37.p13 chr 9	NC_000009.11:g.131175356_131175375=	NC_000009.11:g.131175364_131175375del	NC_000009.11:g.131175369_131175375del	NC_000009.11:g.131175371_131175375del	NC_000009.11:g.131175372_131175375del	NC_000009.11:g.131175373_131175375del	NC_000009.11:g.131175374_131175375del	NC_000009.11:g.131175375del	NC_000009.11:g.131175375dup	NC_000009.11:g.131175374_131175375dup	NC_000009.11:g.131175373_131175375dup	NC_000009.11:g.131175372_131175375dup	NC_000009.11:g.131175371_131175375dup	NC_000009.11:g.131175370_131175375dup
CERCAM transcript variant X1	XM_005252035.1:c.-811+1005=	XM_005252035.1:c.-811+1013_-811+1024del	XM_005252035.1:c.-811+1018_-811+1024del	XM_005252035.1:c.-811+1020_-811+1024del	XM_005252035.1:c.-811+1021_-811+1024del	XM_005252035.1:c.-811+1022_-811+1024del	XM_005252035.1:c.-811+1023_-811+1024del	XM_005252035.1:c.-811+1024del	XM_005252035.1:c.-811+1024dup	XM_005252035.1:c.-811+1023_-811+1024dup	XM_005252035.1:c.-811+1022_-811+1024dup	XM_005252035.1:c.-811+1021_-811+1024dup	XM_005252035.1:c.-811+1020_-811+1024dup	XM_005252035.1:c.-811+1019_-811+1024dup
CERCAM transcript variant X4	XM_005252038.1:c.-157+1005=	XM_005252038.1:c.-157+1013_-157+1024del	XM_005252038.1:c.-157+1018_-157+1024del	XM_005252038.1:c.-157+1020_-157+1024del	XM_005252038.1:c.-157+1021_-157+1024del	XM_005252038.1:c.-157+1022_-157+1024del	XM_005252038.1:c.-157+1023_-157+1024del	XM_005252038.1:c.-157+1024del	XM_005252038.1:c.-157+1024dup	XM_005252038.1:c.-157+1023_-157+1024dup	XM_005252038.1:c.-157+1022_-157+1024dup	XM_005252038.1:c.-157+1021_-157+1024dup	XM_005252038.1:c.-157+1020_-157+1024dup	XM_005252038.1:c.-157+1019_-157+1024dup

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#.

41 SubSNP, 28 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	EVA_GENOME_DK	ss1577470078	Apr 01, 2015 (144)
2	SWEGEN	ss3005644732	Nov 08, 2017 (151)
3	MCHAISSO	ss3064354161	Nov 08, 2017 (151)
4	ACPOP	ss3736903571	Jul 13, 2019 (153)
5	ACPOP	ss3736903572	Jul 13, 2019 (153)
6	PACBIO	ss3796610502	Jul 13, 2019 (153)
7	EVA	ss3831875830	Apr 26, 2020 (154)
8	GNOMAD	ss4210015859	Apr 26, 2021 (155)
9	GNOMAD	ss4210015860	Apr 26, 2021 (155)
10	GNOMAD	ss4210015861	Apr 26, 2021 (155)
11	GNOMAD	ss4210015862	Apr 26, 2021 (155)
12	GNOMAD	ss4210015863	Apr 26, 2021 (155)
13	GNOMAD	ss4210015864	Apr 26, 2021 (155)
14	GNOMAD	ss4210015865	Apr 26, 2021 (155)
15	GNOMAD	ss4210015866	Apr 26, 2021 (155)
16	GNOMAD	ss4210015867	Apr 26, 2021 (155)
17	GNOMAD	ss4210015868	Apr 26, 2021 (155)
18	GNOMAD	ss4210015869	Apr 26, 2021 (155)
19	GNOMAD	ss4210015870	Apr 26, 2021 (155)
20	TOPMED	ss4836857031	Apr 26, 2021 (155)
21	TOMMO_GENOMICS	ss5195452284	Apr 26, 2021 (155)
22	TOMMO_GENOMICS	ss5195452285	Apr 26, 2021 (155)
23	TOMMO_GENOMICS	ss5195452286	Apr 26, 2021 (155)
24	TOMMO_GENOMICS	ss5195452287	Apr 26, 2021 (155)
25	TOMMO_GENOMICS	ss5195452288	Apr 26, 2021 (155)
26	1000G_HIGH_COVERAGE	ss5282294266	Oct 16, 2022 (156)
27	1000G_HIGH_COVERAGE	ss5282294267	Oct 16, 2022 (156)
28	1000G_HIGH_COVERAGE	ss5282294268	Oct 16, 2022 (156)
29	1000G_HIGH_COVERAGE	ss5282294269	Oct 16, 2022 (156)
30	1000G_HIGH_COVERAGE	ss5282294270	Oct 16, 2022 (156)
31	HUGCELL_USP	ss5478151840	Oct 16, 2022 (156)
32	HUGCELL_USP	ss5478151841	Oct 16, 2022 (156)
33	HUGCELL_USP	ss5478151842	Oct 16, 2022 (156)
34	HUGCELL_USP	ss5478151843	Oct 16, 2022 (156)
35	HUGCELL_USP	ss5478151844	Oct 16, 2022 (156)
36	TOMMO_GENOMICS	ss5740030136	Oct 16, 2022 (156)
37	TOMMO_GENOMICS	ss5740030137	Oct 16, 2022 (156)
38	TOMMO_GENOMICS	ss5740030138	Oct 16, 2022 (156)
39	TOMMO_GENOMICS	ss5740030139	Oct 16, 2022 (156)
40	TOMMO_GENOMICS	ss5740030140	Oct 16, 2022 (156)
41	TOMMO_GENOMICS	ss5740030141	Oct 16, 2022 (156)
42	The Danish reference pan genome	NC_000009.11 - 131175356	Apr 26, 2020 (154)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338634547 (NC_000009.12:128413076::T 1060/91636) Row 338634548 (NC_000009.12:128413076::TT 35/91656) Row 338634549 (NC_000009.12:128413076::TTT 9/91656)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338634547 (NC_000009.12:128413076::T 1060/91636) Row 338634548 (NC_000009.12:128413076::TT 35/91656) Row 338634549 (NC_000009.12:128413076::TTT 9/91656)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338634547 (NC_000009.12:128413076::T 1060/91636) Row 338634548 (NC_000009.12:128413076::TT 35/91656) Row 338634549 (NC_000009.12:128413076::TTT 9/91656)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338634547 (NC_000009.12:128413076::T 1060/91636) Row 338634548 (NC_000009.12:128413076::TT 35/91656) Row 338634549 (NC_000009.12:128413076::TTT 9/91656)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338634547 (NC_000009.12:128413076::T 1060/91636) Row 338634548 (NC_000009.12:128413076::TT 35/91656) Row 338634549 (NC_000009.12:128413076::TTT 9/91656)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338634547 (NC_000009.12:128413076::T 1060/91636) Row 338634548 (NC_000009.12:128413076::TT 35/91656) Row 338634549 (NC_000009.12:128413076::TTT 9/91656)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338634547 (NC_000009.12:128413076::T 1060/91636) Row 338634548 (NC_000009.12:128413076::TT 35/91656) Row 338634549 (NC_000009.12:128413076::TTT 9/91656)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338634547 (NC_000009.12:128413076::T 1060/91636) Row 338634548 (NC_000009.12:128413076::TT 35/91656) Row 338634549 (NC_000009.12:128413076::TTT 9/91656)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338634547 (NC_000009.12:128413076::T 1060/91636) Row 338634548 (NC_000009.12:128413076::TT 35/91656) Row 338634549 (NC_000009.12:128413076::TTT 9/91656)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338634547 (NC_000009.12:128413076::T 1060/91636) Row 338634548 (NC_000009.12:128413076::TT 35/91656) Row 338634549 (NC_000009.12:128413076::TTT 9/91656)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338634547 (NC_000009.12:128413076::T 1060/91636) Row 338634548 (NC_000009.12:128413076::TT 35/91656) Row 338634549 (NC_000009.12:128413076::TTT 9/91656)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338634547 (NC_000009.12:128413076::T 1060/91636) Row 338634548 (NC_000009.12:128413076::TT 35/91656) Row 338634549 (NC_000009.12:128413076::TTT 9/91656)...	-	Apr 26, 2021 (155)
55	Northern Sweden Submission ignored due to conflicting rows: Row 10188436 (NC_000009.11:131175355:T: 14/598) Row 10188437 (NC_000009.11:131175355:TT: 4/598)	-	Jul 13, 2019 (153)
56	Northern Sweden Submission ignored due to conflicting rows: Row 10188436 (NC_000009.11:131175355:T: 14/598) Row 10188437 (NC_000009.11:131175355:TT: 4/598)	-	Jul 13, 2019 (153)
57	8.3KJPN Submission ignored due to conflicting rows: Row 53421591 (NC_000009.11:131175355:T: 2115/16140) Row 53421592 (NC_000009.11:131175355:TTTTTTT: 361/16140) Row 53421593 (NC_000009.11:131175355:TT: 1924/16140)...	-	Apr 26, 2021 (155)
58	8.3KJPN Submission ignored due to conflicting rows: Row 53421591 (NC_000009.11:131175355:T: 2115/16140) Row 53421592 (NC_000009.11:131175355:TTTTTTT: 361/16140) Row 53421593 (NC_000009.11:131175355:TT: 1924/16140)...	-	Apr 26, 2021 (155)
59	8.3KJPN Submission ignored due to conflicting rows: Row 53421591 (NC_000009.11:131175355:T: 2115/16140) Row 53421592 (NC_000009.11:131175355:TTTTTTT: 361/16140) Row 53421593 (NC_000009.11:131175355:TT: 1924/16140)...	-	Apr 26, 2021 (155)
60	8.3KJPN Submission ignored due to conflicting rows: Row 53421591 (NC_000009.11:131175355:T: 2115/16140) Row 53421592 (NC_000009.11:131175355:TTTTTTT: 361/16140) Row 53421593 (NC_000009.11:131175355:TT: 1924/16140)...	-	Apr 26, 2021 (155)
61	8.3KJPN Submission ignored due to conflicting rows: Row 53421591 (NC_000009.11:131175355:T: 2115/16140) Row 53421592 (NC_000009.11:131175355:TTTTTTT: 361/16140) Row 53421593 (NC_000009.11:131175355:TT: 1924/16140)...	-	Apr 26, 2021 (155)
62	14KJPN Submission ignored due to conflicting rows: Row 73867240 (NC_000009.12:128413076:TT: 3898/27912) Row 73867241 (NC_000009.12:128413076:T: 4171/27912) Row 73867242 (NC_000009.12:128413076:TTTTTTT: 638/27912)...	-	Oct 16, 2022 (156)
63	14KJPN Submission ignored due to conflicting rows: Row 73867240 (NC_000009.12:128413076:TT: 3898/27912) Row 73867241 (NC_000009.12:128413076:T: 4171/27912) Row 73867242 (NC_000009.12:128413076:TTTTTTT: 638/27912)...	-	Oct 16, 2022 (156)
64	14KJPN Submission ignored due to conflicting rows: Row 73867240 (NC_000009.12:128413076:TT: 3898/27912) Row 73867241 (NC_000009.12:128413076:T: 4171/27912) Row 73867242 (NC_000009.12:128413076:TTTTTTT: 638/27912)...	-	Oct 16, 2022 (156)
65	14KJPN Submission ignored due to conflicting rows: Row 73867240 (NC_000009.12:128413076:TT: 3898/27912) Row 73867241 (NC_000009.12:128413076:T: 4171/27912) Row 73867242 (NC_000009.12:128413076:TTTTTTT: 638/27912)...	-	Oct 16, 2022 (156)
66	14KJPN Submission ignored due to conflicting rows: Row 73867240 (NC_000009.12:128413076:TT: 3898/27912) Row 73867241 (NC_000009.12:128413076:T: 4171/27912) Row 73867242 (NC_000009.12:128413076:TTTTTTT: 638/27912)...	-	Oct 16, 2022 (156)
67	14KJPN Submission ignored due to conflicting rows: Row 73867240 (NC_000009.12:128413076:TT: 3898/27912) Row 73867241 (NC_000009.12:128413076:T: 4171/27912) Row 73867242 (NC_000009.12:128413076:TTTTTTT: 638/27912)...	-	Oct 16, 2022 (156)
68	TopMed	NC_000009.12 - 128413077	Apr 26, 2021 (155)
69	ALFA	NC_000009.12 - 128413077	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
674234592, ss4836857031	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTT:	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTT	(self)
3419961753	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTT	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTT	(self)
ss5195452285	NC_000009.11:131175355:TTTTTTT:	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4210015870, ss5282294270, ss5740030138	NC_000009.12:128413076:TTTTTTT:	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
3419961753	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4210015869	NC_000009.12:128413076:TTTTT:	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4210015868, ss5478151844, ss5740030141	NC_000009.12:128413076:TTTT:	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
3419961753	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3796610502, ss5195452288	NC_000009.11:131175355:TTT:	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4210015867, ss5282294269, ss5478151843, ss5740030140	NC_000009.12:128413076:TTT:	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
3419961753	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3005644732, ss3736903572, ss5195452286	NC_000009.11:131175355:TT:	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3064354161, ss4210015866, ss5282294268, ss5478151842, ss5740030136	NC_000009.12:128413076:TT:	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
3419961753	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
1303736, ss1577470078, ss3736903571, ss3831875830, ss5195452284	NC_000009.11:131175355:T:	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4210015865, ss5282294266, ss5478151841, ss5740030137	NC_000009.12:128413076:T:	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
3419961753	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss5195452287	NC_000009.11:131175355::T	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4210015859, ss5282294267, ss5478151840, ss5740030139	NC_000009.12:128413076::T	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
3419961753	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4210015860	NC_000009.12:128413076::TT	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
3419961753	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4210015861	NC_000009.12:128413076::TTT	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
3419961753	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4210015862	NC_000009.12:128413076::TTTT	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4210015863	NC_000009.12:128413076::TTTTT	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4210015864	NC_000009.12:128413076::TTTTTT	NC_000009.12:128413076:TTTTTTTTTTT… NC_000009.12:128413076:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs756133661

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

rs756133661