Name: rs11412829
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.

rs11412829

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:36161562-36161578 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₇ / del(T)₅ / del(T)₄ / delT…
del(T)₇ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.2797 (1675/5988, ALFA)
dupT=0.4828 (2418/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: BRPF3-AS1 : 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	5988	TTTTTTTTTTTTTTTTT=0.7156	TTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.2797, TTTTTTTTTTTTTTTTTTT=0.0042, TTTTTTTTTTTTTTTTTTTT=0.0005, TTTTTTTTTTTTTTTTTTTTT=0.0000	0.62888	0.187922	0.183198	32
European	Sub	5752	TTTTTTTTTTTTTTTTT=0.7050	TTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.2902, TTTTTTTTTTTTTTTTTTT=0.0043, TTTTTTTTTTTTTTTTTTTT=0.0005, TTTTTTTTTTTTTTTTTTTTT=0.0000	0.614547	0.194659	0.190794	32
African	Sub	94	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African Others	Sub	2	TTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
African American	Sub	92	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Asian	Sub	8	TTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	4	TTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	4	TTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	12	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	42	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	12	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	68	TTTTTTTTTTTTTTTTT=0.91	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.09, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	0.911765	0.088235	0.0	19

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	5988	(T)₁₇=0.7156	del(T)₇=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.2797, dupTT=0.0042, dupTTT=0.0005, dup(T)₄=0.0000
Allele Frequency Aggregator	European	Sub	5752	(T)₁₇=0.7050	del(T)₇=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.2902, dupTT=0.0043, dupTTT=0.0005, dup(T)₄=0.0000
Allele Frequency Aggregator	African	Sub	94	(T)₁₇=1.00	del(T)₇=0.00, del(T)₅=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, dup(T)₄=0.00
Allele Frequency Aggregator	Other	Sub	68	(T)₁₇=0.91	del(T)₇=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.09, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	Latin American 2	Sub	42	(T)₁₇=1.00	del(T)₇=0.00, del(T)₅=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, dup(T)₄=0.00
Allele Frequency Aggregator	Latin American 1	Sub	12	(T)₁₇=1.00	del(T)₇=0.00, del(T)₅=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, dup(T)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	12	(T)₁₇=1.00	del(T)₇=0.00, del(T)₅=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, dup(T)₄=0.00
Allele Frequency Aggregator	Asian	Sub	8	(T)₁₇=1.0	del(T)₇=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupT=0.4828
1000Genomes	African	Sub	1322	- No frequency provided	dupT=0.5265
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupT=0.4891
1000Genomes	Europe	Sub	1006	- No frequency provided	dupT=0.4076
1000Genomes	South Asian	Sub	978	- No frequency provided	dupT=0.488
1000Genomes	American	Sub	694	- No frequency provided	dupT=0.493

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 6	NC_000006.12:g.36161572_36161578del
GRCh38.p14 chr 6	NC_000006.12:g.36161574_36161578del
GRCh38.p14 chr 6	NC_000006.12:g.36161575_36161578del
GRCh38.p14 chr 6	NC_000006.12:g.36161576_36161578del
GRCh38.p14 chr 6	NC_000006.12:g.36161577_36161578del
GRCh38.p14 chr 6	NC_000006.12:g.36161578del
GRCh38.p14 chr 6	NC_000006.12:g.36161578dup
GRCh38.p14 chr 6	NC_000006.12:g.36161577_36161578dup
GRCh38.p14 chr 6	NC_000006.12:g.36161576_36161578dup
GRCh38.p14 chr 6	NC_000006.12:g.36161575_36161578dup
GRCh37.p13 chr 6	NC_000006.11:g.36129349_36129355del
GRCh37.p13 chr 6	NC_000006.11:g.36129351_36129355del
GRCh37.p13 chr 6	NC_000006.11:g.36129352_36129355del
GRCh37.p13 chr 6	NC_000006.11:g.36129353_36129355del
GRCh37.p13 chr 6	NC_000006.11:g.36129354_36129355del
GRCh37.p13 chr 6	NC_000006.11:g.36129355del
GRCh37.p13 chr 6	NC_000006.11:g.36129355dup
GRCh37.p13 chr 6	NC_000006.11:g.36129354_36129355dup
GRCh37.p13 chr 6	NC_000006.11:g.36129353_36129355dup
GRCh37.p13 chr 6	NC_000006.11:g.36129352_36129355dup

Gene: BRPF3-AS1, uncharacterized BRPF3-AS1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
BRPF3-AS1 transcript variant X6	XR_001744105.2:n.	N/A	Intron Variant
BRPF3-AS1 transcript variant X1	XR_427918.4:n.	N/A	Intron Variant
BRPF3-AS1 transcript variant X2	XR_926750.3:n.	N/A	Intron Variant
BRPF3-AS1 transcript variant X3	XR_926752.3:n.	N/A	Intron Variant
BRPF3-AS1 transcript variant X4	XR_926753.3:n.	N/A	Intron Variant
BRPF3-AS1 transcript variant X5	XR_926754.2: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)₁₇=	del(T)₇	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄
GRCh38.p14 chr 6	NC_000006.12:g.36161562_36161578=	NC_000006.12:g.36161572_36161578del	NC_000006.12:g.36161574_36161578del	NC_000006.12:g.36161575_36161578del	NC_000006.12:g.36161576_36161578del	NC_000006.12:g.36161577_36161578del	NC_000006.12:g.36161578del	NC_000006.12:g.36161578dup	NC_000006.12:g.36161577_36161578dup	NC_000006.12:g.36161576_36161578dup	NC_000006.12:g.36161575_36161578dup
GRCh37.p13 chr 6	NC_000006.11:g.36129339_36129355=	NC_000006.11:g.36129349_36129355del	NC_000006.11:g.36129351_36129355del	NC_000006.11:g.36129352_36129355del	NC_000006.11:g.36129353_36129355del	NC_000006.11:g.36129354_36129355del	NC_000006.11:g.36129355del	NC_000006.11:g.36129355dup	NC_000006.11:g.36129354_36129355dup	NC_000006.11:g.36129353_36129355dup	NC_000006.11:g.36129352_36129355dup

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#.

59 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42805364	Mar 13, 2006 (138)
2	HGSV	ss81795814	Oct 12, 2018 (152)
3	HUMANGENOME_JCVI	ss98453548	Feb 04, 2009 (138)
4	BCMHGSC_JDW	ss103728519	Dec 01, 2009 (131)
5	GMI	ss288700839	May 04, 2012 (137)
6	PJP	ss295275245	May 09, 2011 (137)
7	PJP	ss295275246	May 09, 2011 (137)
8	SSMP	ss663692313	Apr 01, 2015 (144)
9	BILGI_BIOE	ss666350745	Apr 25, 2013 (138)
10	1000GENOMES	ss1375377636	Aug 21, 2014 (142)
11	SWEGEN	ss2998891085	Nov 08, 2017 (151)
12	EVA_DECODE	ss3716997092	Jul 13, 2019 (153)
13	EVA_DECODE	ss3716997093	Jul 13, 2019 (153)
14	EVA_DECODE	ss3716997094	Jul 13, 2019 (153)
15	EVA_DECODE	ss3716997095	Jul 13, 2019 (153)
16	PACBIO	ss3785445797	Jul 13, 2019 (153)
17	PACBIO	ss3790801545	Jul 13, 2019 (153)
18	PACBIO	ss3795680171	Jul 13, 2019 (153)
19	PACBIO	ss3795680172	Jul 13, 2019 (153)
20	KHV_HUMAN_GENOMES	ss3808038157	Jul 13, 2019 (153)
21	EVA	ss3829868048	Apr 26, 2020 (154)
22	EVA	ss3838411279	Apr 26, 2020 (154)
23	EVA	ss3843855405	Apr 26, 2020 (154)
24	KOGIC	ss3958808026	Apr 26, 2020 (154)
25	KOGIC	ss3958808027	Apr 26, 2020 (154)
26	KOGIC	ss3958808028	Apr 26, 2020 (154)
27	GNOMAD	ss4139905147	Apr 26, 2021 (155)
28	GNOMAD	ss4139905148	Apr 26, 2021 (155)
29	GNOMAD	ss4139905149	Apr 26, 2021 (155)
30	GNOMAD	ss4139905150	Apr 26, 2021 (155)
31	GNOMAD	ss4139905152	Apr 26, 2021 (155)
32	GNOMAD	ss4139905153	Apr 26, 2021 (155)
33	GNOMAD	ss4139905154	Apr 26, 2021 (155)
34	GNOMAD	ss4139905155	Apr 26, 2021 (155)
35	GNOMAD	ss4139905156	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5177026429	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5177026430	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5177026431	Apr 26, 2021 (155)
39	1000G_HIGH_COVERAGE	ss5268067044	Oct 13, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5268067045	Oct 13, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5268067046	Oct 13, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5268067047	Oct 13, 2022 (156)
43	HUGCELL_USP	ss5465776678	Oct 13, 2022 (156)
44	HUGCELL_USP	ss5465776679	Oct 13, 2022 (156)
45	HUGCELL_USP	ss5465776680	Oct 13, 2022 (156)
46	HUGCELL_USP	ss5465776681	Oct 13, 2022 (156)
47	TOMMO_GENOMICS	ss5714932772	Oct 13, 2022 (156)
48	TOMMO_GENOMICS	ss5714932773	Oct 13, 2022 (156)
49	TOMMO_GENOMICS	ss5714932774	Oct 13, 2022 (156)
50	EVA	ss5842092266	Oct 13, 2022 (156)
51	EVA	ss5842092267	Oct 13, 2022 (156)
52	EVA	ss5855311971	Oct 13, 2022 (156)
53	EVA	ss5883380134	Oct 13, 2022 (156)
54	EVA	ss5935808464	Oct 13, 2022 (156)
55	EVA	ss5935808465	Oct 13, 2022 (156)
56	EVA	ss5935808466	Oct 13, 2022 (156)
57	EVA	ss5935808467	Oct 13, 2022 (156)
58	EVA	ss5935808468	Oct 13, 2022 (156)
59	EVA	ss5935808469	Oct 13, 2022 (156)
60	1000Genomes	NC_000006.11 - 36129339	Oct 12, 2018 (152)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222118910 (NC_000006.12:36161561::T 77620/118920) Row 222118911 (NC_000006.12:36161561::TT 1822/118804) Row 222118912 (NC_000006.12:36161561::TTT 186/118910)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222118910 (NC_000006.12:36161561::T 77620/118920) Row 222118911 (NC_000006.12:36161561::TT 1822/118804) Row 222118912 (NC_000006.12:36161561::TTT 186/118910)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222118910 (NC_000006.12:36161561::T 77620/118920) Row 222118911 (NC_000006.12:36161561::TT 1822/118804) Row 222118912 (NC_000006.12:36161561::TTT 186/118910)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222118910 (NC_000006.12:36161561::T 77620/118920) Row 222118911 (NC_000006.12:36161561::TT 1822/118804) Row 222118912 (NC_000006.12:36161561::TTT 186/118910)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222118910 (NC_000006.12:36161561::T 77620/118920) Row 222118911 (NC_000006.12:36161561::TT 1822/118804) Row 222118912 (NC_000006.12:36161561::TTT 186/118910)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222118910 (NC_000006.12:36161561::T 77620/118920) Row 222118911 (NC_000006.12:36161561::TT 1822/118804) Row 222118912 (NC_000006.12:36161561::TTT 186/118910)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222118910 (NC_000006.12:36161561::T 77620/118920) Row 222118911 (NC_000006.12:36161561::TT 1822/118804) Row 222118912 (NC_000006.12:36161561::TTT 186/118910)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222118910 (NC_000006.12:36161561::T 77620/118920) Row 222118911 (NC_000006.12:36161561::TT 1822/118804) Row 222118912 (NC_000006.12:36161561::TTT 186/118910)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222118910 (NC_000006.12:36161561::T 77620/118920) Row 222118911 (NC_000006.12:36161561::TT 1822/118804) Row 222118912 (NC_000006.12:36161561::TTT 186/118910)...	-	Apr 26, 2021 (155)
70	Korean Genome Project Submission ignored due to conflicting rows: Row 15186027 (NC_000006.12:36161562::T 928/1830) Row 15186028 (NC_000006.12:36161562::TT 86/1830) Row 15186029 (NC_000006.12:36161561:T: 73/1830)	-	Apr 26, 2020 (154)
71	Korean Genome Project Submission ignored due to conflicting rows: Row 15186027 (NC_000006.12:36161562::T 928/1830) Row 15186028 (NC_000006.12:36161562::TT 86/1830) Row 15186029 (NC_000006.12:36161561:T: 73/1830)	-	Apr 26, 2020 (154)
72	Korean Genome Project Submission ignored due to conflicting rows: Row 15186027 (NC_000006.12:36161562::T 928/1830) Row 15186028 (NC_000006.12:36161562::TT 86/1830) Row 15186029 (NC_000006.12:36161561:T: 73/1830)	-	Apr 26, 2020 (154)
73	8.3KJPN Submission ignored due to conflicting rows: Row 34995736 (NC_000006.11:36129338::T 11273/16718) Row 34995737 (NC_000006.11:36129338:T: 20/16718) Row 34995738 (NC_000006.11:36129338::TT 154/16718)	-	Apr 26, 2021 (155)
74	8.3KJPN Submission ignored due to conflicting rows: Row 34995736 (NC_000006.11:36129338::T 11273/16718) Row 34995737 (NC_000006.11:36129338:T: 20/16718) Row 34995738 (NC_000006.11:36129338::TT 154/16718)	-	Apr 26, 2021 (155)
75	8.3KJPN Submission ignored due to conflicting rows: Row 34995736 (NC_000006.11:36129338::T 11273/16718) Row 34995737 (NC_000006.11:36129338:T: 20/16718) Row 34995738 (NC_000006.11:36129338::TT 154/16718)	-	Apr 26, 2021 (155)
76	14KJPN Submission ignored due to conflicting rows: Row 48769876 (NC_000006.12:36161561::T 19241/28258) Row 48769877 (NC_000006.12:36161561:T: 34/28258) Row 48769878 (NC_000006.12:36161561::TT 272/28258)	-	Oct 13, 2022 (156)
77	14KJPN Submission ignored due to conflicting rows: Row 48769876 (NC_000006.12:36161561::T 19241/28258) Row 48769877 (NC_000006.12:36161561:T: 34/28258) Row 48769878 (NC_000006.12:36161561::TT 272/28258)	-	Oct 13, 2022 (156)
78	14KJPN Submission ignored due to conflicting rows: Row 48769876 (NC_000006.12:36161561::T 19241/28258) Row 48769877 (NC_000006.12:36161561:T: 34/28258) Row 48769878 (NC_000006.12:36161561::TT 272/28258)	-	Oct 13, 2022 (156)
79	ALFA	NC_000006.12 - 36161562	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)
rs34416739	May 15, 2013 (138)
rs35733867	May 11, 2012 (137)
rs56852663	May 11, 2012 (137)
rs66533156	May 11, 2012 (137)
rs67293142	May 11, 2012 (137)
rs67293143	Feb 27, 2009 (130)
rs67293144	Feb 27, 2009 (130)
rs67781396	May 11, 2012 (137)
rs67781397	Feb 27, 2009 (130)
rs137934841	Sep 17, 2011 (135)
rs147351242	Sep 17, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4139905156	NC_000006.12:36161561:TTTTTTT:	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
11107706050	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
11107706050	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4139905155	NC_000006.12:36161561:TTTT:	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
11107706050	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss5935808467	NC_000006.11:36129338:TTT:	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT
ss4139905154	NC_000006.12:36161561:TTT:	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
11107706050	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss5935808466	NC_000006.11:36129338:TT:	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT
ss3716997092, ss4139905153, ss5465776681	NC_000006.12:36161561:TT:	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
11107706050	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss103728519	NT_007592.15:36069353:TT:	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss2998891085, ss5177026430, ss5935808465	NC_000006.11:36129338:T:	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3958808028, ss4139905152, ss5268067046, ss5465776680, ss5714932773	NC_000006.12:36161561:T:	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
11107706050	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3716997093	NC_000006.12:36161562:T:	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss295275245	NC_000006.10:36237317::T	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss288700839, ss295275246	NC_000006.10:36237333::T	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
31471833, ss663692313, ss666350745, ss1375377636, ss3785445797, ss3790801545, ss3795680171, ss3829868048, ss3838411279, ss5177026429, ss5842092266, ss5935808464	NC_000006.11:36129338::T	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3808038157, ss3843855405, ss4139905147, ss5268067044, ss5465776678, ss5714932772, ss5855311971, ss5883380134	NC_000006.12:36161561::T	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
11107706050	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3958808026	NC_000006.12:36161562::T	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3716997094	NC_000006.12:36161563::T	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss42805364, ss98453548	NT_007592.15:36069338::T	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss81795814	NT_007592.15:36069355::T	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3795680172, ss5177026431, ss5842092267, ss5935808468	NC_000006.11:36129338::TT	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4139905148, ss5268067045, ss5465776679, ss5714932774	NC_000006.12:36161561::TT	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
11107706050	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3958808027	NC_000006.12:36161562::TT	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3716997095	NC_000006.12:36161563::TT	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss5935808469	NC_000006.11:36129338::TTT	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT
ss4139905149, ss5268067047	NC_000006.12:36161561::TTT	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
11107706050	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4139905150	NC_000006.12:36161561::TTTT	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
11107706050	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000006.12:36161561:TTTTTTTTTTTT… NC_000006.12:36161561:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(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 rs11412829

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

rs11412829