Name: rs34341899
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.

rs34341899

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:191259201-191259212 (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: delTT / delT / dupT / dupTT / dupT…
delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₁₂
Variation Type: Indel Insertion and Deletion
Frequency: dupTTT=0.1728 (1164/6738, ALFA)
delT=0.1472 (737/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: OSTN : 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	6738	TTTTTTTTTTTT=0.6575	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.1646, TTTTTTTTTTTTTTT=0.1728, TTTTTTTTTTTTT=0.0037, TTTTTTTTTTTTTTTT=0.0009, TTTTTTTTTTTTTT=0.0006, TTTTTTTTTTTTTTTTT=0.0000	0.725954	0.101161	0.172886	32
European	Sub	5588	TTTTTTTTTTTT=0.5880	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.1981, TTTTTTTTTTTTTTT=0.2076, TTTTTTTTTTTTT=0.0045, TTTTTTTTTTTTTTTT=0.0011, TTTTTTTTTTTTTT=0.0007, TTTTTTTTTTTTTTTTT=0.0000	0.641653	0.132137	0.22621	32
African	Sub	848	TTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	42	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	806	TTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	66	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	48	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	18	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	12	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	86	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	20	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	118	TTTTTTTTTTTT=0.949	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.017, TTTTTTTTTTTTTTT=0.034, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000	0.964912	0.017544	0.017544	14

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	6738	(T)₁₂=0.6575	delTT=0.0000, delT=0.1646, dupT=0.0037, dupTT=0.0006, dupTTT=0.1728, dup(T)₄=0.0009, dup(T)₅=0.0000
Allele Frequency Aggregator	European	Sub	5588	(T)₁₂=0.5880	delTT=0.0000, delT=0.1981, dupT=0.0045, dupTT=0.0007, dupTTT=0.2076, dup(T)₄=0.0011, dup(T)₅=0.0000
Allele Frequency Aggregator	African	Sub	848	(T)₁₂=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000
Allele Frequency Aggregator	Other	Sub	118	(T)₁₂=0.949	delTT=0.000, delT=0.017, dupT=0.000, dupTT=0.000, dupTTT=0.034, dup(T)₄=0.000, dup(T)₅=0.000
Allele Frequency Aggregator	Latin American 2	Sub	86	(T)₁₂=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00
Allele Frequency Aggregator	Asian	Sub	66	(T)₁₂=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	20	(T)₁₂=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00
Allele Frequency Aggregator	Latin American 1	Sub	12	(T)₁₂=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00
1000Genomes	Global	Study-wide	5008	(T)₁₂=0.7151	delT=0.1472, dupT=0.1378
1000Genomes	African	Sub	1322	(T)₁₂=0.7428	delT=0.0885, dupT=0.1687
1000Genomes	East Asian	Sub	1008	(T)₁₂=0.9196	delT=0.0486, dupT=0.0317
1000Genomes	Europe	Sub	1006	(T)₁₂=0.6024	delT=0.1968, dupT=0.2008
1000Genomes	South Asian	Sub	978	(T)₁₂=0.630	delT=0.224, dupT=0.146
1000Genomes	American	Sub	694	(T)₁₂=0.648	delT=0.222, dupT=0.130

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 3	NC_000003.12:g.191259211_191259212del
GRCh38.p14 chr 3	NC_000003.12:g.191259212del
GRCh38.p14 chr 3	NC_000003.12:g.191259212dup
GRCh38.p14 chr 3	NC_000003.12:g.191259211_191259212dup
GRCh38.p14 chr 3	NC_000003.12:g.191259210_191259212dup
GRCh38.p14 chr 3	NC_000003.12:g.191259209_191259212dup
GRCh38.p14 chr 3	NC_000003.12:g.191259208_191259212dup
GRCh38.p14 chr 3	NC_000003.12:g.191259207_191259212dup
GRCh38.p14 chr 3	NC_000003.12:g.191259206_191259212dup
GRCh38.p14 chr 3	NC_000003.12:g.191259201_191259212dup
GRCh37.p13 chr 3	NC_000003.11:g.190977000_190977001del
GRCh37.p13 chr 3	NC_000003.11:g.190977001del
GRCh37.p13 chr 3	NC_000003.11:g.190977001dup
GRCh37.p13 chr 3	NC_000003.11:g.190977000_190977001dup
GRCh37.p13 chr 3	NC_000003.11:g.190976999_190977001dup
GRCh37.p13 chr 3	NC_000003.11:g.190976998_190977001dup
GRCh37.p13 chr 3	NC_000003.11:g.190976997_190977001dup
GRCh37.p13 chr 3	NC_000003.11:g.190976996_190977001dup
GRCh37.p13 chr 3	NC_000003.11:g.190976995_190977001dup
GRCh37.p13 chr 3	NC_000003.11:g.190976990_190977001dup

Gene: OSTN, osteocrin (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
OSTN transcript	NM_198184.2:c.13-3655_1… NM_198184.2:c.13-3655_13-3654del	N/A	Intron Variant
OSTN transcript variant X1	XM_017006303.3:c.13-3655… XM_017006303.3:c.13-3655_*13-3654del	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)₁₂=	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₁₂
GRCh38.p14 chr 3	NC_000003.12:g.191259201_191259212=	NC_000003.12:g.191259211_191259212del	NC_000003.12:g.191259212del	NC_000003.12:g.191259212dup	NC_000003.12:g.191259211_191259212dup	NC_000003.12:g.191259210_191259212dup	NC_000003.12:g.191259209_191259212dup	NC_000003.12:g.191259208_191259212dup	NC_000003.12:g.191259207_191259212dup	NC_000003.12:g.191259206_191259212dup	NC_000003.12:g.191259201_191259212dup
GRCh37.p13 chr 3	NC_000003.11:g.190976990_190977001=	NC_000003.11:g.190977000_190977001del	NC_000003.11:g.190977001del	NC_000003.11:g.190977001dup	NC_000003.11:g.190977000_190977001dup	NC_000003.11:g.190976999_190977001dup	NC_000003.11:g.190976998_190977001dup	NC_000003.11:g.190976997_190977001dup	NC_000003.11:g.190976996_190977001dup	NC_000003.11:g.190976995_190977001dup	NC_000003.11:g.190976990_190977001dup
OSTN transcript	NM_198184.2:c.*13-3665=	NM_198184.2:c.13-3655_13-3654del	NM_198184.2:c.*13-3654del	NM_198184.2:c.*13-3654dup	NM_198184.2:c.13-3655_13-3654dup	NM_198184.2:c.13-3656_13-3654dup	NM_198184.2:c.13-3657_13-3654dup	NM_198184.2:c.13-3658_13-3654dup	NM_198184.2:c.13-3659_13-3654dup	NM_198184.2:c.13-3660_13-3654dup	NM_198184.2:c.13-3665_13-3654dup
OSTN transcript variant X1	XM_005247428.1:c.*13-3665=	XM_005247428.1:c.13-3655_13-3654del	XM_005247428.1:c.*13-3654del	XM_005247428.1:c.*13-3654dup	XM_005247428.1:c.13-3655_13-3654dup	XM_005247428.1:c.13-3656_13-3654dup	XM_005247428.1:c.13-3657_13-3654dup	XM_005247428.1:c.13-3658_13-3654dup	XM_005247428.1:c.13-3659_13-3654dup	XM_005247428.1:c.13-3660_13-3654dup	XM_005247428.1:c.13-3665_13-3654dup
OSTN transcript variant X1	XM_017006303.3:c.*13-3665=	XM_017006303.3:c.13-3655_13-3654del	XM_017006303.3:c.*13-3654del	XM_017006303.3:c.*13-3654dup	XM_017006303.3:c.13-3655_13-3654dup	XM_017006303.3:c.13-3656_13-3654dup	XM_017006303.3:c.13-3657_13-3654dup	XM_017006303.3:c.13-3658_13-3654dup	XM_017006303.3:c.13-3659_13-3654dup	XM_017006303.3:c.13-3660_13-3654dup	XM_017006303.3:c.13-3665_13-3654dup

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#.

76 SubSNP, 34 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41855118	Mar 15, 2006 (126)
2	ABI	ss41936633	Mar 13, 2006 (126)
3	ABI	ss42064966	Mar 13, 2006 (126)
4	HGSV	ss82331830	Dec 15, 2007 (130)
5	HUMANGENOME_JCVI	ss95342267	Feb 06, 2009 (130)
6	GMI	ss288466560	May 04, 2012 (137)
7	PJP	ss295146378	May 09, 2011 (137)
8	PJP	ss295146379	May 09, 2011 (134)
9	TISHKOFF	ss554045599	Apr 25, 2013 (138)
10	SSMP	ss663390855	Apr 01, 2015 (144)
11	BILGI_BIOE	ss666241097	Apr 25, 2013 (138)
12	1000GENOMES	ss1371529701	Aug 21, 2014 (142)
13	1000GENOMES	ss1371529704	Oct 12, 2018 (152)
14	DDI	ss1536388956	Apr 01, 2015 (144)
15	EVA_UK10K_ALSPAC	ss1703988309	Apr 01, 2015 (144)
16	EVA_UK10K_TWINSUK	ss1703988330	Apr 01, 2015 (144)
17	EVA_UK10K_ALSPAC	ss1710125333	Oct 12, 2018 (152)
18	EVA_UK10K_TWINSUK	ss1710125334	Oct 12, 2018 (152)
19	HAMMER_LAB	ss1800670018	Sep 08, 2015 (146)
20	SWEGEN	ss2993863801	Nov 08, 2017 (151)
21	BIOINF_KMB_FNS_UNIBA	ss3645767393	Oct 12, 2018 (152)
22	URBANLAB	ss3647615864	Oct 12, 2018 (152)
23	EVA_DECODE	ss3711099423	Jul 13, 2019 (153)
24	EVA_DECODE	ss3711099424	Jul 13, 2019 (153)
25	EVA_DECODE	ss3711099425	Jul 13, 2019 (153)
26	EVA_DECODE	ss3711099426	Jul 13, 2019 (153)
27	EVA_DECODE	ss3711099427	Jul 13, 2019 (153)
28	EVA_DECODE	ss3711099428	Jul 13, 2019 (153)
29	ACPOP	ss3730714387	Jul 13, 2019 (153)
30	ACPOP	ss3730714388	Jul 13, 2019 (153)
31	ACPOP	ss3730714389	Jul 13, 2019 (153)
32	ACPOP	ss3730714390	Jul 13, 2019 (153)
33	PACBIO	ss3784574582	Jul 13, 2019 (153)
34	PACBIO	ss3790050376	Jul 13, 2019 (153)
35	PACBIO	ss3790050377	Jul 13, 2019 (153)
36	PACBIO	ss3794925206	Jul 13, 2019 (153)
37	PACBIO	ss3794925207	Jul 13, 2019 (153)
38	KHV_HUMAN_GENOMES	ss3804339561	Jul 13, 2019 (153)
39	KHV_HUMAN_GENOMES	ss3804339562	Jul 13, 2019 (153)
40	EVA	ss3828289146	Apr 25, 2020 (154)
41	EVA	ss3837576432	Apr 25, 2020 (154)
42	EVA	ss3843009318	Apr 25, 2020 (154)
43	KOGIC	ss3953210876	Apr 25, 2020 (154)
44	KOGIC	ss3953210877	Apr 25, 2020 (154)
45	KOGIC	ss3953210878	Apr 25, 2020 (154)
46	KOGIC	ss3953210879	Apr 25, 2020 (154)
47	KOGIC	ss3953210880	Apr 25, 2020 (154)
48	GNOMAD	ss4088097159	Apr 26, 2021 (155)
49	GNOMAD	ss4088097160	Apr 26, 2021 (155)
50	GNOMAD	ss4088097161	Apr 26, 2021 (155)
51	GNOMAD	ss4088097162	Apr 26, 2021 (155)
52	GNOMAD	ss4088097163	Apr 26, 2021 (155)
53	GNOMAD	ss4088097164	Apr 26, 2021 (155)
54	GNOMAD	ss4088097166	Apr 26, 2021 (155)
55	TOMMO_GENOMICS	ss5163469708	Apr 26, 2021 (155)
56	TOMMO_GENOMICS	ss5163469709	Apr 26, 2021 (155)
57	TOMMO_GENOMICS	ss5163469710	Apr 26, 2021 (155)
58	TOMMO_GENOMICS	ss5163469711	Apr 26, 2021 (155)
59	TOMMO_GENOMICS	ss5163469712	Apr 26, 2021 (155)
60	1000G_HIGH_COVERAGE	ss5257486968	Oct 13, 2022 (156)
61	1000G_HIGH_COVERAGE	ss5257486969	Oct 13, 2022 (156)
62	1000G_HIGH_COVERAGE	ss5257486970	Oct 13, 2022 (156)
63	1000G_HIGH_COVERAGE	ss5257486971	Oct 13, 2022 (156)
64	HUGCELL_USP	ss5456486027	Oct 13, 2022 (156)
65	HUGCELL_USP	ss5456486028	Oct 13, 2022 (156)
66	HUGCELL_USP	ss5456486029	Oct 13, 2022 (156)
67	HUGCELL_USP	ss5456486030	Oct 13, 2022 (156)
68	TOMMO_GENOMICS	ss5696890437	Oct 13, 2022 (156)
69	TOMMO_GENOMICS	ss5696890438	Oct 13, 2022 (156)
70	TOMMO_GENOMICS	ss5696890439	Oct 13, 2022 (156)
71	TOMMO_GENOMICS	ss5696890440	Oct 13, 2022 (156)
72	TOMMO_GENOMICS	ss5696890441	Oct 13, 2022 (156)
73	TOMMO_GENOMICS	ss5696890442	Oct 13, 2022 (156)
74	EVA	ss5827044637	Oct 13, 2022 (156)
75	EVA	ss5827044638	Oct 13, 2022 (156)
76	EVA	ss5827044639	Oct 13, 2022 (156)
77	1000Genomes	NC_000003.11 - 190976990	Oct 12, 2018 (152)
78	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 10677519 (NC_000003.11:190976989::TTT 1368/3854) Row 10677520 (NC_000003.11:190976989:T: 913/3854)	-	Oct 12, 2018 (152)
79	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 10677519 (NC_000003.11:190976989::TTT 1368/3854) Row 10677520 (NC_000003.11:190976989:T: 913/3854)	-	Oct 12, 2018 (152)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 135981789 (NC_000003.12:191259200::T 2713/135532) Row 135981790 (NC_000003.12:191259200::TT 86/135580) Row 135981791 (NC_000003.12:191259200::TTT 44660/135332)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 135981789 (NC_000003.12:191259200::T 2713/135532) Row 135981790 (NC_000003.12:191259200::TT 86/135580) Row 135981791 (NC_000003.12:191259200::TTT 44660/135332)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 135981789 (NC_000003.12:191259200::T 2713/135532) Row 135981790 (NC_000003.12:191259200::TT 86/135580) Row 135981791 (NC_000003.12:191259200::TTT 44660/135332)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 135981789 (NC_000003.12:191259200::T 2713/135532) Row 135981790 (NC_000003.12:191259200::TT 86/135580) Row 135981791 (NC_000003.12:191259200::TTT 44660/135332)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 135981789 (NC_000003.12:191259200::T 2713/135532) Row 135981790 (NC_000003.12:191259200::TT 86/135580) Row 135981791 (NC_000003.12:191259200::TTT 44660/135332)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 135981789 (NC_000003.12:191259200::T 2713/135532) Row 135981790 (NC_000003.12:191259200::TT 86/135580) Row 135981791 (NC_000003.12:191259200::TTT 44660/135332)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 135981789 (NC_000003.12:191259200::T 2713/135532) Row 135981790 (NC_000003.12:191259200::TT 86/135580) Row 135981791 (NC_000003.12:191259200::TTT 44660/135332)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 135981789 (NC_000003.12:191259200::T 2713/135532) Row 135981790 (NC_000003.12:191259200::TT 86/135580) Row 135981791 (NC_000003.12:191259200::TTT 44660/135332)...	-	Apr 26, 2021 (155)
88	Korean Genome Project Submission ignored due to conflicting rows: Row 9588877 (NC_000003.12:191259201::T 350/1832) Row 9588878 (NC_000003.12:191259201::TT 5/1832) Row 9588879 (NC_000003.12:191259200:T: 149/1832)...	-	Apr 25, 2020 (154)
89	Korean Genome Project Submission ignored due to conflicting rows: Row 9588877 (NC_000003.12:191259201::T 350/1832) Row 9588878 (NC_000003.12:191259201::TT 5/1832) Row 9588879 (NC_000003.12:191259200:T: 149/1832)...	-	Apr 25, 2020 (154)
90	Korean Genome Project Submission ignored due to conflicting rows: Row 9588877 (NC_000003.12:191259201::T 350/1832) Row 9588878 (NC_000003.12:191259201::TT 5/1832) Row 9588879 (NC_000003.12:191259200:T: 149/1832)...	-	Apr 25, 2020 (154)
91	Korean Genome Project Submission ignored due to conflicting rows: Row 9588877 (NC_000003.12:191259201::T 350/1832) Row 9588878 (NC_000003.12:191259201::TT 5/1832) Row 9588879 (NC_000003.12:191259200:T: 149/1832)...	-	Apr 25, 2020 (154)
92	Korean Genome Project Submission ignored due to conflicting rows: Row 9588877 (NC_000003.12:191259201::T 350/1832) Row 9588878 (NC_000003.12:191259201::TT 5/1832) Row 9588879 (NC_000003.12:191259200:T: 149/1832)...	-	Apr 25, 2020 (154)
93	Northern Sweden Submission ignored due to conflicting rows: Row 3999252 (NC_000003.11:190976989:T: 143/594) Row 3999253 (NC_000003.11:190976989::TTT 121/594) Row 3999254 (NC_000003.11:190976989::T 8/594)...	-	Jul 13, 2019 (153)
94	Northern Sweden Submission ignored due to conflicting rows: Row 3999252 (NC_000003.11:190976989:T: 143/594) Row 3999253 (NC_000003.11:190976989::TTT 121/594) Row 3999254 (NC_000003.11:190976989::T 8/594)...	-	Jul 13, 2019 (153)
95	Northern Sweden Submission ignored due to conflicting rows: Row 3999252 (NC_000003.11:190976989:T: 143/594) Row 3999253 (NC_000003.11:190976989::TTT 121/594) Row 3999254 (NC_000003.11:190976989::T 8/594)...	-	Jul 13, 2019 (153)
96	Northern Sweden Submission ignored due to conflicting rows: Row 3999252 (NC_000003.11:190976989:T: 143/594) Row 3999253 (NC_000003.11:190976989::TTT 121/594) Row 3999254 (NC_000003.11:190976989::T 8/594)...	-	Jul 13, 2019 (153)
97	8.3KJPN Submission ignored due to conflicting rows: Row 21439015 (NC_000003.11:190976989:T: 1718/16760) Row 21439016 (NC_000003.11:190976989::TTT 825/16760) Row 21439017 (NC_000003.11:190976989::T 2886/16760)...	-	Apr 26, 2021 (155)
98	8.3KJPN Submission ignored due to conflicting rows: Row 21439015 (NC_000003.11:190976989:T: 1718/16760) Row 21439016 (NC_000003.11:190976989::TTT 825/16760) Row 21439017 (NC_000003.11:190976989::T 2886/16760)...	-	Apr 26, 2021 (155)
99	8.3KJPN Submission ignored due to conflicting rows: Row 21439015 (NC_000003.11:190976989:T: 1718/16760) Row 21439016 (NC_000003.11:190976989::TTT 825/16760) Row 21439017 (NC_000003.11:190976989::T 2886/16760)...	-	Apr 26, 2021 (155)
100	8.3KJPN Submission ignored due to conflicting rows: Row 21439015 (NC_000003.11:190976989:T: 1718/16760) Row 21439016 (NC_000003.11:190976989::TTT 825/16760) Row 21439017 (NC_000003.11:190976989::T 2886/16760)...	-	Apr 26, 2021 (155)
101	8.3KJPN Submission ignored due to conflicting rows: Row 21439015 (NC_000003.11:190976989:T: 1718/16760) Row 21439016 (NC_000003.11:190976989::TTT 825/16760) Row 21439017 (NC_000003.11:190976989::T 2886/16760)...	-	Apr 26, 2021 (155)
102	14KJPN Submission ignored due to conflicting rows: Row 30727541 (NC_000003.12:191259200::T 4924/28258) Row 30727542 (NC_000003.12:191259200:T: 2915/28258) Row 30727543 (NC_000003.12:191259200::TTT 1420/28258)...	-	Oct 13, 2022 (156)
103	14KJPN Submission ignored due to conflicting rows: Row 30727541 (NC_000003.12:191259200::T 4924/28258) Row 30727542 (NC_000003.12:191259200:T: 2915/28258) Row 30727543 (NC_000003.12:191259200::TTT 1420/28258)...	-	Oct 13, 2022 (156)
104	14KJPN Submission ignored due to conflicting rows: Row 30727541 (NC_000003.12:191259200::T 4924/28258) Row 30727542 (NC_000003.12:191259200:T: 2915/28258) Row 30727543 (NC_000003.12:191259200::TTT 1420/28258)...	-	Oct 13, 2022 (156)
105	14KJPN Submission ignored due to conflicting rows: Row 30727541 (NC_000003.12:191259200::T 4924/28258) Row 30727542 (NC_000003.12:191259200:T: 2915/28258) Row 30727543 (NC_000003.12:191259200::TTT 1420/28258)...	-	Oct 13, 2022 (156)
106	14KJPN Submission ignored due to conflicting rows: Row 30727541 (NC_000003.12:191259200::T 4924/28258) Row 30727542 (NC_000003.12:191259200:T: 2915/28258) Row 30727543 (NC_000003.12:191259200::TTT 1420/28258)...	-	Oct 13, 2022 (156)
107	14KJPN Submission ignored due to conflicting rows: Row 30727541 (NC_000003.12:191259200::T 4924/28258) Row 30727542 (NC_000003.12:191259200:T: 2915/28258) Row 30727543 (NC_000003.12:191259200::TTT 1420/28258)...	-	Oct 13, 2022 (156)
108	UK 10K study - Twins Submission ignored due to conflicting rows: Row 10677519 (NC_000003.11:190976989::TTT 1309/3708) Row 10677520 (NC_000003.11:190976989:T: 884/3708)	-	Oct 12, 2018 (152)
109	UK 10K study - Twins Submission ignored due to conflicting rows: Row 10677519 (NC_000003.11:190976989::TTT 1309/3708) Row 10677520 (NC_000003.11:190976989:T: 884/3708)	-	Oct 12, 2018 (152)
110	ALFA	NC_000003.12 - 191259201	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)
rs151093864	May 11, 2012 (137)
rs377230809	May 15, 2013 (138)
rs34404667	Oct 15, 2006 (127)
rs35535419	Oct 15, 2006 (127)
rs58224091	May 26, 2008 (130)
rs373305489	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4088097166, ss5696890441	NC_000003.12:191259200:TT:	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTT	(self)
11835902082	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTT	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTT	(self)
ss288466560	NC_000003.10:192459683:T:	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
19148523, ss1371529701, ss1703988309, ss1703988330, ss2993863801, ss3730714387, ss5163469708, ss5827044639	NC_000003.11:190976989:T:	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss554045599	NC_000003.11:190977000:T:	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3645767393, ss3711099423, ss3804339562, ss3953210878, ss5257486968, ss5456486027, ss5696890438	NC_000003.12:191259200:T:	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
11835902082	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTT	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3730714389, ss5163469710	NC_000003.11:190976989::T	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
19148523	NC_000003.11:190976989:T:TT	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4088097159, ss5257486969, ss5456486029, ss5696890437	NC_000003.12:191259200::T	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
11835902082	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3953210876	NC_000003.12:191259201::T	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss41936633	NT_005612.16:97472145::T	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss41855118	NT_005612.16:97472146::T	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss42064966	NT_005612.16:97472147::T	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3790050376, ss3794925206, ss5163469711	NC_000003.11:190976989::TT	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4088097160, ss5696890440	NC_000003.12:191259200::TT	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
11835902082	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3711099424, ss3953210877	NC_000003.12:191259201::TT	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss295146378	NC_000003.10:192459684::TTT	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss295146379	NC_000003.10:192459693::TTT	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss663390855, ss666241097, ss1536388956, ss1800670018, ss3730714388, ss3784574582, ss3790050377, ss3794925207, ss3828289146, ss3837576432, ss5163469709, ss5827044637	NC_000003.11:190976989::TTT	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss1371529704, ss1710125333, ss1710125334	NC_000003.11:190976990::TTT	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3647615864, ss3843009318, ss4088097161, ss5257486970, ss5456486028, ss5696890439	NC_000003.12:191259200::TTT	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
11835902082	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3711099425, ss3804339561, ss3953210879	NC_000003.12:191259201::TTT	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss82331830, ss95342267	NT_005612.16:97472147::TTT	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3730714390, ss5163469712, ss5827044638	NC_000003.11:190976989::TTTT	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4088097162, ss5257486971, ss5456486030, ss5696890442	NC_000003.12:191259200::TTTT	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
11835902082	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3711099426, ss3953210880	NC_000003.12:191259201::TTTT	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4088097163	NC_000003.12:191259200::TTTTT	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
11835902082	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4088097164	NC_000003.12:191259200::TTTTTT	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3711099427	NC_000003.12:191259201::TTTTTTT	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3711099428	NC_000003.12:191259201::TTTTTTTTTT… NC_000003.12:191259201::TTTTTTTTTTTT	NC_000003.12:191259200:TTTTTTTTTTT… NC_000003.12:191259200:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(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 rs34341899

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

rs34341899