Name: rs71045956
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.

rs71045956

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr11:66653363-66653379 (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 / dupTTT / dup(T)₄ / dup(T)₆ / dup(T)₁₀
Variation Type: Indel Insertion and Deletion
Frequency: (T)₁₇=0.4880 (2444/5008, 1000G)
dupTT=0.1124 (501/4456, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: RBM4 : 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	4456	TTTTTTTTTTTTTTTTT=0.0900	TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0004, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.7971, TTTTTTTTTTTTTTTTTTT=0.1124, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.797506	0.046883	0.155611	32
European	Sub	4450	TTTTTTTTTTTTTTTTT=0.0901	TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0004, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.7975, TTTTTTTTTTTTTTTTTTT=0.1119, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.798202	0.046454	0.155345	32
African	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
African Others	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
African American	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Asian	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
East Asian	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Other Asian	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 2	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
South Asian	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Other	Sub	6	TTTTTTTTTTTTTTTTT=0.0	TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.5, TTTTTTTTTTTTTTTTTTT=0.5, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0	0.333333	0.333333	0.333333	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
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupT=0.5120
1000Genomes	African	Sub	1322	- No frequency provided	dupT=0.4917
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupT=0.5179
1000Genomes	Europe	Sub	1006	- No frequency provided	dupT=0.5417
1000Genomes	South Asian	Sub	978	- No frequency provided	dupT=0.475
1000Genomes	American	Sub	694	- No frequency provided	dupT=0.550
Allele Frequency Aggregator	Total	Global	4456	(T)₁₇=0.0900	delTTT=0.0000, delTT=0.0004, delT=0.0000, dupT=0.7971, dupTT=0.1124, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₆=0.0000
Allele Frequency Aggregator	European	Sub	4450	(T)₁₇=0.0901	delTTT=0.0000, delTT=0.0004, delT=0.0000, dupT=0.7975, dupTT=0.1119, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₆=0.0000
Allele Frequency Aggregator	Other	Sub	6	(T)₁₇=0.0	delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.5, dupTT=0.5, dupTTT=0.0, dup(T)₄=0.0, dup(T)₆=0.0
Allele Frequency Aggregator	Latin American 1	Sub	0	(T)₁₇=0	delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0, dup(T)₄=0, dup(T)₆=0
Allele Frequency Aggregator	Latin American 2	Sub	0	(T)₁₇=0	delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0, dup(T)₄=0, dup(T)₆=0
Allele Frequency Aggregator	South Asian	Sub	0	(T)₁₇=0	delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0, dup(T)₄=0, dup(T)₆=0
Allele Frequency Aggregator	African	Sub	0	(T)₁₇=0	delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0, dup(T)₄=0, dup(T)₆=0
Allele Frequency Aggregator	Asian	Sub	0	(T)₁₇=0	delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0, dup(T)₄=0, dup(T)₆=0

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 11	NC_000011.10:g.66653376_66653379del
GRCh38.p14 chr 11	NC_000011.10:g.66653377_66653379del
GRCh38.p14 chr 11	NC_000011.10:g.66653378_66653379del
GRCh38.p14 chr 11	NC_000011.10:g.66653379del
GRCh38.p14 chr 11	NC_000011.10:g.66653379dup
GRCh38.p14 chr 11	NC_000011.10:g.66653378_66653379dup
GRCh38.p14 chr 11	NC_000011.10:g.66653377_66653379dup
GRCh38.p14 chr 11	NC_000011.10:g.66653376_66653379dup
GRCh38.p14 chr 11	NC_000011.10:g.66653374_66653379dup
GRCh38.p14 chr 11	NC_000011.10:g.66653370_66653379dup
GRCh37.p13 chr 11	NC_000011.9:g.66420847_66420850del
GRCh37.p13 chr 11	NC_000011.9:g.66420848_66420850del
GRCh37.p13 chr 11	NC_000011.9:g.66420849_66420850del
GRCh37.p13 chr 11	NC_000011.9:g.66420850del
GRCh37.p13 chr 11	NC_000011.9:g.66420850dup
GRCh37.p13 chr 11	NC_000011.9:g.66420849_66420850dup
GRCh37.p13 chr 11	NC_000011.9:g.66420848_66420850dup
GRCh37.p13 chr 11	NC_000011.9:g.66420847_66420850dup
GRCh37.p13 chr 11	NC_000011.9:g.66420845_66420850dup
GRCh37.p13 chr 11	NC_000011.9:g.66420841_66420850dup

Gene: RBM4, RNA binding motif protein 4 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
RBM4 transcript variant 3	NM_001198844.2:c.413-1248… NM_001198844.2:c.413-12480_413-12477del	N/A	Intron Variant
RBM4 transcript variant 2	NM_001198843.2:c.	N/A	Genic Downstream Transcript Variant
RBM4 transcript variant 1	NM_002896.4:c.	N/A	Genic Downstream Transcript Variant

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

Not Reported in ClinVar

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

Placement	(T)₁₇=	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₆	dup(T)₁₀
GRCh38.p14 chr 11	NC_000011.10:g.66653363_66653379=	NC_000011.10:g.66653376_66653379del	NC_000011.10:g.66653377_66653379del	NC_000011.10:g.66653378_66653379del	NC_000011.10:g.66653379del	NC_000011.10:g.66653379dup	NC_000011.10:g.66653378_66653379dup	NC_000011.10:g.66653377_66653379dup	NC_000011.10:g.66653376_66653379dup	NC_000011.10:g.66653374_66653379dup	NC_000011.10:g.66653370_66653379dup
GRCh37.p13 chr 11	NC_000011.9:g.66420834_66420850=	NC_000011.9:g.66420847_66420850del	NC_000011.9:g.66420848_66420850del	NC_000011.9:g.66420849_66420850del	NC_000011.9:g.66420850del	NC_000011.9:g.66420850dup	NC_000011.9:g.66420849_66420850dup	NC_000011.9:g.66420848_66420850dup	NC_000011.9:g.66420847_66420850dup	NC_000011.9:g.66420845_66420850dup	NC_000011.9:g.66420841_66420850dup
RBM4 transcript variant 3	NM_001198844.1:c.413-12493=	NM_001198844.1:c.413-12480_413-12477del	NM_001198844.1:c.413-12479_413-12477del	NM_001198844.1:c.413-12478_413-12477del	NM_001198844.1:c.413-12477del	NM_001198844.1:c.413-12477dup	NM_001198844.1:c.413-12478_413-12477dup	NM_001198844.1:c.413-12479_413-12477dup	NM_001198844.1:c.413-12480_413-12477dup	NM_001198844.1:c.413-12482_413-12477dup	NM_001198844.1:c.413-12486_413-12477dup
RBM4 transcript variant 3	NM_001198844.2:c.413-12493=	NM_001198844.2:c.413-12480_413-12477del	NM_001198844.2:c.413-12479_413-12477del	NM_001198844.2:c.413-12478_413-12477del	NM_001198844.2:c.413-12477del	NM_001198844.2:c.413-12477dup	NM_001198844.2:c.413-12478_413-12477dup	NM_001198844.2:c.413-12479_413-12477dup	NM_001198844.2:c.413-12480_413-12477dup	NM_001198844.2:c.413-12482_413-12477dup	NM_001198844.2:c.413-12486_413-12477dup
RBM4 transcript variant X2	XM_005274146.1:c.*8+9223=	XM_005274146.1:c.8+9236_8+9239del	XM_005274146.1:c.8+9237_8+9239del	XM_005274146.1:c.8+9238_8+9239del	XM_005274146.1:c.*8+9239del	XM_005274146.1:c.*8+9239dup	XM_005274146.1:c.8+9238_8+9239dup	XM_005274146.1:c.8+9237_8+9239dup	XM_005274146.1:c.8+9236_8+9239dup	XM_005274146.1:c.8+9234_8+9239dup	XM_005274146.1:c.8+9230_8+9239dup

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#.

50 SubSNP, 25 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95571329	Dec 05, 2013 (144)
2	PJP	ss294707546	May 09, 2011 (137)
3	PJP	ss294707547	May 09, 2011 (135)
4	BILGI_BIOE	ss666538480	Apr 25, 2013 (138)
5	1000GENOMES	ss1371050180	Aug 21, 2014 (142)
6	EVA_UK10K_ALSPAC	ss1707138321	Apr 01, 2015 (144)
7	EVA_UK10K_ALSPAC	ss1707138323	Apr 01, 2015 (144)
8	EVA_UK10K_ALSPAC	ss1707138324	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1707138416	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1707138417	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1707138418	Apr 01, 2015 (144)
12	SWEGEN	ss3008252869	Nov 08, 2017 (151)
13	SWEGEN	ss3008252870	Nov 08, 2017 (151)
14	SWEGEN	ss3008252871	Nov 08, 2017 (151)
15	EVA_DECODE	ss3691973112	Jul 13, 2019 (153)
16	EVA_DECODE	ss3691973113	Jul 13, 2019 (153)
17	EVA_DECODE	ss3691973114	Jul 13, 2019 (153)
18	EVA_DECODE	ss3691973115	Jul 13, 2019 (153)
19	EVA_DECODE	ss3691973116	Jul 13, 2019 (153)
20	PACBIO	ss3786979222	Jul 13, 2019 (153)
21	PACBIO	ss3792116533	Jul 13, 2019 (153)
22	PACBIO	ss3796998878	Jul 13, 2019 (153)
23	KHV_HUMAN_GENOMES	ss3814754631	Jul 13, 2019 (153)
24	EVA	ss3832675591	Apr 26, 2020 (154)
25	GNOMAD	ss4236772312	Apr 26, 2021 (155)
26	GNOMAD	ss4236772313	Apr 26, 2021 (155)
27	GNOMAD	ss4236772314	Apr 26, 2021 (155)
28	GNOMAD	ss4236772315	Apr 26, 2021 (155)
29	GNOMAD	ss4236772316	Apr 26, 2021 (155)
30	GNOMAD	ss4236772318	Apr 26, 2021 (155)
31	GNOMAD	ss4236772319	Apr 26, 2021 (155)
32	GNOMAD	ss4236772320	Apr 26, 2021 (155)
33	GNOMAD	ss4236772321	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5202425757	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5202425758	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5202425759	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5202425760	Apr 26, 2021 (155)
38	1000G_HIGH_COVERAGE	ss5287758313	Oct 16, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5287758314	Oct 16, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5287758315	Oct 16, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5287758316	Oct 16, 2022 (156)
42	HUGCELL_USP	ss5482895938	Oct 16, 2022 (156)
43	HUGCELL_USP	ss5482895939	Oct 16, 2022 (156)
44	TOMMO_GENOMICS	ss5750443038	Oct 16, 2022 (156)
45	TOMMO_GENOMICS	ss5750443039	Oct 16, 2022 (156)
46	TOMMO_GENOMICS	ss5750443040	Oct 16, 2022 (156)
47	TOMMO_GENOMICS	ss5750443041	Oct 16, 2022 (156)
48	EVA	ss5836790511	Oct 16, 2022 (156)
49	EVA	ss5836790512	Oct 16, 2022 (156)
50	EVA	ss5836790513	Oct 16, 2022 (156)
51	1000Genomes	NC_000011.9 - 66420834	Oct 12, 2018 (152)
52	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 30092467 (NC_000011.9:66420833::T 3110/3854) Row 30092468 (NC_000011.9:66420833::TTT 91/3854) Row 30092469 (NC_000011.9:66420833::TT 571/3854)	-	Oct 12, 2018 (152)
53	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 30092467 (NC_000011.9:66420833::T 3110/3854) Row 30092468 (NC_000011.9:66420833::TTT 91/3854) Row 30092469 (NC_000011.9:66420833::TT 571/3854)	-	Oct 12, 2018 (152)
54	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 30092467 (NC_000011.9:66420833::T 3110/3854) Row 30092468 (NC_000011.9:66420833::TTT 91/3854) Row 30092469 (NC_000011.9:66420833::TT 571/3854)	-	Oct 12, 2018 (152)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 382570906 (NC_000011.10:66653362::T 115097/124798) Row 382570907 (NC_000011.10:66653362::TT 8149/124702) Row 382570908 (NC_000011.10:66653362::TTT 42/124742)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 382570906 (NC_000011.10:66653362::T 115097/124798) Row 382570907 (NC_000011.10:66653362::TT 8149/124702) Row 382570908 (NC_000011.10:66653362::TTT 42/124742)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 382570906 (NC_000011.10:66653362::T 115097/124798) Row 382570907 (NC_000011.10:66653362::TT 8149/124702) Row 382570908 (NC_000011.10:66653362::TTT 42/124742)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 382570906 (NC_000011.10:66653362::T 115097/124798) Row 382570907 (NC_000011.10:66653362::TT 8149/124702) Row 382570908 (NC_000011.10:66653362::TTT 42/124742)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 382570906 (NC_000011.10:66653362::T 115097/124798) Row 382570907 (NC_000011.10:66653362::TT 8149/124702) Row 382570908 (NC_000011.10:66653362::TTT 42/124742)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 382570906 (NC_000011.10:66653362::T 115097/124798) Row 382570907 (NC_000011.10:66653362::TT 8149/124702) Row 382570908 (NC_000011.10:66653362::TTT 42/124742)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 382570906 (NC_000011.10:66653362::T 115097/124798) Row 382570907 (NC_000011.10:66653362::TT 8149/124702) Row 382570908 (NC_000011.10:66653362::TTT 42/124742)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 382570906 (NC_000011.10:66653362::T 115097/124798) Row 382570907 (NC_000011.10:66653362::TT 8149/124702) Row 382570908 (NC_000011.10:66653362::TTT 42/124742)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 382570906 (NC_000011.10:66653362::T 115097/124798) Row 382570907 (NC_000011.10:66653362::TT 8149/124702) Row 382570908 (NC_000011.10:66653362::TTT 42/124742)...	-	Apr 26, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 60395064 (NC_000011.9:66420833::TT 1579/16682) Row 60395065 (NC_000011.9:66420833::T 14806/16682) Row 60395066 (NC_000011.9:66420833:TT: 1/16682)...	-	Apr 26, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 60395064 (NC_000011.9:66420833::TT 1579/16682) Row 60395065 (NC_000011.9:66420833::T 14806/16682) Row 60395066 (NC_000011.9:66420833:TT: 1/16682)...	-	Apr 26, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 60395064 (NC_000011.9:66420833::TT 1579/16682) Row 60395065 (NC_000011.9:66420833::T 14806/16682) Row 60395066 (NC_000011.9:66420833:TT: 1/16682)...	-	Apr 26, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 60395064 (NC_000011.9:66420833::TT 1579/16682) Row 60395065 (NC_000011.9:66420833::T 14806/16682) Row 60395066 (NC_000011.9:66420833:TT: 1/16682)...	-	Apr 26, 2021 (155)
68	14KJPN Submission ignored due to conflicting rows: Row 84280142 (NC_000011.10:66653362::T 24823/28128) Row 84280143 (NC_000011.10:66653362::TT 2537/28128) Row 84280144 (NC_000011.10:66653362:TT: 1/28128)...	-	Oct 16, 2022 (156)
69	14KJPN Submission ignored due to conflicting rows: Row 84280142 (NC_000011.10:66653362::T 24823/28128) Row 84280143 (NC_000011.10:66653362::TT 2537/28128) Row 84280144 (NC_000011.10:66653362:TT: 1/28128)...	-	Oct 16, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 84280142 (NC_000011.10:66653362::T 24823/28128) Row 84280143 (NC_000011.10:66653362::TT 2537/28128) Row 84280144 (NC_000011.10:66653362:TT: 1/28128)...	-	Oct 16, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 84280142 (NC_000011.10:66653362::T 24823/28128) Row 84280143 (NC_000011.10:66653362::TT 2537/28128) Row 84280144 (NC_000011.10:66653362:TT: 1/28128)...	-	Oct 16, 2022 (156)
72	UK 10K study - Twins Submission ignored due to conflicting rows: Row 30092467 (NC_000011.9:66420833::T 2962/3708) Row 30092468 (NC_000011.9:66420833::TTT 85/3708) Row 30092469 (NC_000011.9:66420833::TT 576/3708)	-	Oct 12, 2018 (152)
73	UK 10K study - Twins Submission ignored due to conflicting rows: Row 30092467 (NC_000011.9:66420833::T 2962/3708) Row 30092468 (NC_000011.9:66420833::TTT 85/3708) Row 30092469 (NC_000011.9:66420833::TT 576/3708)	-	Oct 12, 2018 (152)
74	UK 10K study - Twins Submission ignored due to conflicting rows: Row 30092467 (NC_000011.9:66420833::T 2962/3708) Row 30092468 (NC_000011.9:66420833::TTT 85/3708) Row 30092469 (NC_000011.9:66420833::TT 576/3708)	-	Oct 12, 2018 (152)
75	ALFA	NC_000011.10 - 66653363	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)
rs72046976	May 11, 2012 (137)
rs72074192	May 11, 2012 (137)
rs137884198	Sep 17, 2011 (135)
rs145303745	Sep 17, 2011 (135)
rs398016475	Jul 01, 2015 (144)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4236772321	NC_000011.10:66653362:TTTT:	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4236772320, ss5287758315	NC_000011.10:66653362:TTT:	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
3966357463	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss5202425759	NC_000011.9:66420833:TT:	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4236772319, ss5287758314, ss5750443040	NC_000011.10:66653362:TT:	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
3966357463	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3691973112, ss4236772318	NC_000011.10:66653362:T:	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
3966357463	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss294707546	NC_000011.8:66177410::T	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss294707547	NC_000011.8:66177426::T	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
54196159, ss666538480, ss1371050180, ss1707138321, ss1707138416, ss3008252869, ss3786979222, ss3792116533, ss3796998878, ss3832675591, ss5202425758, ss5836790511	NC_000011.9:66420833::T	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3814754631, ss4236772312, ss5287758313, ss5482895938, ss5750443038	NC_000011.10:66653362::T	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
3966357463	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3691973113	NC_000011.10:66653363::T	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss95571329	NT_167190.1:11726645::T	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss1707138324, ss1707138418, ss3008252870, ss5202425757, ss5836790512	NC_000011.9:66420833::TT	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4236772313, ss5482895939, ss5750443039	NC_000011.10:66653362::TT	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
3966357463	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3691973114	NC_000011.10:66653363::TT	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss1707138323, ss1707138417, ss3008252871, ss5202425760, ss5836790513	NC_000011.9:66420833::TTT	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4236772314, ss5287758316, ss5750443041	NC_000011.10:66653362::TTT	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
3966357463	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4236772315	NC_000011.10:66653362::TTTT	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
3966357463	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4236772316	NC_000011.10:66653362::TTTTTT	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
3966357463	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3691973115	NC_000011.10:66653363::TTTTTT	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3691973116	NC_000011.10:66653363::TTTTTTTTTT	NC_000011.10:66653362:TTTTTTTTTTTT… NC_000011.10:66653362:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs71045956

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

rs71045956