Name: rs34724351
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.

rs34724351

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:154152903-154152919 (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 / dup(T)₁₀
Variation Type: Indel Insertion and Deletion
Frequency: delTT=0.3598 (2023/5622, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: OPRM1 : 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	5622	TTTTTTTTTTTTTTTTT=0.5336	TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0004, TTTTTTTTTTTTTTT=0.3598, TTTTTTTTTTTTTTTT=0.0733, TTTTTTTTTTTTTTTTTT=0.0329, TTTTTTTTTTTTTTTTTTT=0.0000	0.458462	0.225934	0.315604	32
European	Sub	5186	TTTTTTTTTTTTTTTTT=0.4954	TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0004, TTTTTTTTTTTTTTT=0.3893, TTTTTTTTTTTTTTTT=0.0794, TTTTTTTTTTTTTTTTTT=0.0355, TTTTTTTTTTTTTTTTTTT=0.0000	0.402332	0.249271	0.348397	32
African	Sub	166	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	6	TTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
African American	Sub	160	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	2	TTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	2	TTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 2	Sub	180	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	10	TTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other	Sub	78	TTTTTTTTTTTTTTTTT=0.94	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.05, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.01, TTTTTTTTTTTTTTTTTTT=0.00	0.947368	0.026316	0.026316	9

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	5622	(T)₁₇=0.5336	del(T)₄=0.0000, delTTT=0.0004, delTT=0.3598, delT=0.0733, dupT=0.0329, dupTT=0.0000
Allele Frequency Aggregator	European	Sub	5186	(T)₁₇=0.4954	del(T)₄=0.0000, delTTT=0.0004, delTT=0.3893, delT=0.0794, dupT=0.0355, dupTT=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	180	(T)₁₇=1.000	del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	African	Sub	166	(T)₁₇=1.000	del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Other	Sub	78	(T)₁₇=0.94	del(T)₄=0.00, delTTT=0.00, delTT=0.05, delT=0.00, dupT=0.01, dupTT=0.00
Allele Frequency Aggregator	South Asian	Sub	10	(T)₁₇=1.0	del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0
Allele Frequency Aggregator	Asian	Sub	2	(T)₁₇=1.0	del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0
Allele Frequency Aggregator	Latin American 1	Sub	0	(T)₁₇=0	del(T)₄=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=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 6	NC_000006.12:g.154152916_154152919del
GRCh38.p14 chr 6	NC_000006.12:g.154152917_154152919del
GRCh38.p14 chr 6	NC_000006.12:g.154152918_154152919del
GRCh38.p14 chr 6	NC_000006.12:g.154152919del
GRCh38.p14 chr 6	NC_000006.12:g.154152919dup
GRCh38.p14 chr 6	NC_000006.12:g.154152918_154152919dup
GRCh38.p14 chr 6	NC_000006.12:g.154152910_154152919dup
GRCh37.p13 chr 6	NC_000006.11:g.154474051_154474054del
GRCh37.p13 chr 6	NC_000006.11:g.154474052_154474054del
GRCh37.p13 chr 6	NC_000006.11:g.154474053_154474054del
GRCh37.p13 chr 6	NC_000006.11:g.154474054del
GRCh37.p13 chr 6	NC_000006.11:g.154474054dup
GRCh37.p13 chr 6	NC_000006.11:g.154474053_154474054dup
GRCh37.p13 chr 6	NC_000006.11:g.154474045_154474054dup
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.147416_147419del
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.147417_147419del
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.147418_147419del
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.147419del
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.147419dup
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.147418_147419dup
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.147410_147419dup

Gene: OPRM1, opioid receptor mu 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
OPRM1 transcript variant MOR-1O	NM_001008503.3:c.1164+614… NM_001008503.3:c.1164+61444_1164+61447del	N/A	Intron Variant
OPRM1 transcript variant MOR-1	NM_000914.5:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1A	NM_001008504.4:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1X	NM_001008505.2:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1i	NM_001145279.4:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1G1	NM_001145280.4:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1G2	NM_001145281.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1B1	NM_001145282.2:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1B2	NM_001145283.2:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1B3	NM_001145284.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1B4	NM_001145285.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1B5	NM_001145286.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1K1	NM_001145287.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1S	NM_001285522.1:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1A2	NM_001285523.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1CA	NM_001285524.1:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1K2	NM_001285526.2:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1W	NM_001285527.1:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-3	NM_001285528.2:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1Y3	NR_104348.1:n.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1Y2	NR_104349.1:n.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1Z	NR_104350.1:n.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1Y	NR_104351.1:n.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant X2	XM_011535851.4:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant X3	XM_011535853.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant X5	XM_011535856.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant X7	XM_011535862.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant X1	XM_017010903.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant X4	XM_017010904.2:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant X8	XM_017010907.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant X6	XM_047418837.1: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	dup(T)₁₀
GRCh38.p14 chr 6	NC_000006.12:g.154152903_154152919=	NC_000006.12:g.154152916_154152919del	NC_000006.12:g.154152917_154152919del	NC_000006.12:g.154152918_154152919del	NC_000006.12:g.154152919del	NC_000006.12:g.154152919dup	NC_000006.12:g.154152918_154152919dup	NC_000006.12:g.154152910_154152919dup
GRCh37.p13 chr 6	NC_000006.11:g.154474038_154474054=	NC_000006.11:g.154474051_154474054del	NC_000006.11:g.154474052_154474054del	NC_000006.11:g.154474053_154474054del	NC_000006.11:g.154474054del	NC_000006.11:g.154474054dup	NC_000006.11:g.154474053_154474054dup	NC_000006.11:g.154474045_154474054dup
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.147403_147419=	NG_021208.2:g.147416_147419del	NG_021208.2:g.147417_147419del	NG_021208.2:g.147418_147419del	NG_021208.2:g.147419del	NG_021208.2:g.147419dup	NG_021208.2:g.147418_147419dup	NG_021208.2:g.147410_147419dup
OPRM1 transcript variant MOR-1O	NM_001008503.1:c.1164+61431=	NM_001008503.1:c.1164+61444_1164+61447del	NM_001008503.1:c.1164+61445_1164+61447del	NM_001008503.1:c.1164+61446_1164+61447del	NM_001008503.1:c.1164+61447del	NM_001008503.1:c.1164+61447dup	NM_001008503.1:c.1164+61446_1164+61447dup	NM_001008503.1:c.1164+61438_1164+61447dup
OPRM1 transcript variant MOR-1O	NM_001008503.3:c.1164+61431=	NM_001008503.3:c.1164+61444_1164+61447del	NM_001008503.3:c.1164+61445_1164+61447del	NM_001008503.3:c.1164+61446_1164+61447del	NM_001008503.3:c.1164+61447del	NM_001008503.3:c.1164+61447dup	NM_001008503.3:c.1164+61446_1164+61447dup	NM_001008503.3:c.1164+61438_1164+61447dup

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#.

53 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42791262	Dec 03, 2013 (138)
2	HGSV	ss80905164	Dec 14, 2007 (129)
3	HUMANGENOME_JCVI	ss95446324	Dec 05, 2013 (138)
4	BCMHGSC_JDW	ss103741789	Mar 15, 2016 (147)
5	BUSHMAN	ss193894629	Jul 04, 2010 (137)
6	GMI	ss288810921	May 04, 2012 (137)
7	PJP	ss295315046	Aug 21, 2014 (142)
8	BILGI_BIOE	ss666379757	Apr 25, 2013 (138)
9	EVA_UK10K_ALSPAC	ss1705432597	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1705432673	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1710301947	Apr 01, 2015 (144)
12	EVA_UK10K_ALSPAC	ss1710301949	Apr 01, 2015 (144)
13	HAMMER_LAB	ss1804749692	Sep 08, 2015 (146)
14	HAMMER_LAB	ss1804749693	Sep 08, 2015 (146)
15	SWEGEN	ss3000223700	Nov 08, 2017 (151)
16	BIOINF_KMB_FNS_UNIBA	ss3645996336	Oct 12, 2018 (152)
17	URBANLAB	ss3648505423	Oct 12, 2018 (152)
18	EVA_DECODE	ss3718616159	Jul 13, 2019 (153)
19	EVA_DECODE	ss3718616160	Jul 13, 2019 (153)
20	EVA_DECODE	ss3718616161	Jul 13, 2019 (153)
21	EVA_DECODE	ss3718616162	Jul 13, 2019 (153)
22	EVA_DECODE	ss3718616163	Jul 13, 2019 (153)
23	ACPOP	ss3734134142	Jul 13, 2019 (153)
24	ACPOP	ss3734134143	Jul 13, 2019 (153)
25	ACPOP	ss3734134144	Jul 13, 2019 (153)
26	PACBIO	ss3785665487	Jul 13, 2019 (153)
27	PACBIO	ss3790985558	Jul 13, 2019 (153)
28	PACBIO	ss3790985559	Jul 13, 2019 (153)
29	PACBIO	ss3795864943	Jul 13, 2019 (153)
30	EVA	ss3830279683	Apr 26, 2020 (154)
31	GNOMAD	ss4154400984	Apr 26, 2021 (155)
32	GNOMAD	ss4154400985	Apr 26, 2021 (155)
33	GNOMAD	ss4154400987	Apr 26, 2021 (155)
34	GNOMAD	ss4154400988	Apr 26, 2021 (155)
35	GNOMAD	ss4154400989	Apr 26, 2021 (155)
36	GNOMAD	ss4154400990	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5180698221	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5180698222	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5180698223	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5180698224	Apr 26, 2021 (155)
41	1000G_HIGH_COVERAGE	ss5270956790	Oct 14, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5270956791	Oct 14, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5270956792	Oct 14, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5270956793	Oct 14, 2022 (156)
45	HUGCELL_USP	ss5468347025	Oct 14, 2022 (156)
46	HUGCELL_USP	ss5468347026	Oct 14, 2022 (156)
47	HUGCELL_USP	ss5468347027	Oct 14, 2022 (156)
48	TOMMO_GENOMICS	ss5719799500	Oct 14, 2022 (156)
49	TOMMO_GENOMICS	ss5719799501	Oct 14, 2022 (156)
50	TOMMO_GENOMICS	ss5719799502	Oct 14, 2022 (156)
51	TOMMO_GENOMICS	ss5719799503	Oct 14, 2022 (156)
52	EVA	ss5843226432	Oct 14, 2022 (156)
53	EVA	ss5843226433	Oct 14, 2022 (156)
54	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 19438333 (NC_000006.11:154474037:TTT: 303/3854) Row 19438334 (NC_000006.11:154474038:T: 2882/3854)	-	Oct 12, 2018 (152)
55	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 19438333 (NC_000006.11:154474037:TTT: 303/3854) Row 19438334 (NC_000006.11:154474038:T: 2882/3854)	-	Oct 12, 2018 (152)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246107047 (NC_000006.12:154152902::T 3289/132442) Row 246107048 (NC_000006.12:154152902::TT 14/132462) Row 246107050 (NC_000006.12:154152902:T: 15071/132322)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246107047 (NC_000006.12:154152902::T 3289/132442) Row 246107048 (NC_000006.12:154152902::TT 14/132462) Row 246107050 (NC_000006.12:154152902:T: 15071/132322)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246107047 (NC_000006.12:154152902::T 3289/132442) Row 246107048 (NC_000006.12:154152902::TT 14/132462) Row 246107050 (NC_000006.12:154152902:T: 15071/132322)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246107047 (NC_000006.12:154152902::T 3289/132442) Row 246107048 (NC_000006.12:154152902::TT 14/132462) Row 246107050 (NC_000006.12:154152902:T: 15071/132322)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246107047 (NC_000006.12:154152902::T 3289/132442) Row 246107048 (NC_000006.12:154152902::TT 14/132462) Row 246107050 (NC_000006.12:154152902:T: 15071/132322)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246107047 (NC_000006.12:154152902::T 3289/132442) Row 246107048 (NC_000006.12:154152902::TT 14/132462) Row 246107050 (NC_000006.12:154152902:T: 15071/132322)...	-	Apr 26, 2021 (155)
62	Northern Sweden Submission ignored due to conflicting rows: Row 7419007 (NC_000006.11:154474037:TT: 314/586) Row 7419008 (NC_000006.11:154474037:T: 49/586) Row 7419009 (NC_000006.11:154474037::T 14/586)	-	Jul 13, 2019 (153)
63	Northern Sweden Submission ignored due to conflicting rows: Row 7419007 (NC_000006.11:154474037:TT: 314/586) Row 7419008 (NC_000006.11:154474037:T: 49/586) Row 7419009 (NC_000006.11:154474037::T 14/586)	-	Jul 13, 2019 (153)
64	Northern Sweden Submission ignored due to conflicting rows: Row 7419007 (NC_000006.11:154474037:TT: 314/586) Row 7419008 (NC_000006.11:154474037:T: 49/586) Row 7419009 (NC_000006.11:154474037::T 14/586)	-	Jul 13, 2019 (153)
65	8.3KJPN Submission ignored due to conflicting rows: Row 38667528 (NC_000006.11:154474037:T: 7753/16750) Row 38667529 (NC_000006.11:154474037:TT: 8259/16750) Row 38667530 (NC_000006.11:154474037:TTT: 22/16750)...	-	Apr 26, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 38667528 (NC_000006.11:154474037:T: 7753/16750) Row 38667529 (NC_000006.11:154474037:TT: 8259/16750) Row 38667530 (NC_000006.11:154474037:TTT: 22/16750)...	-	Apr 26, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 38667528 (NC_000006.11:154474037:T: 7753/16750) Row 38667529 (NC_000006.11:154474037:TT: 8259/16750) Row 38667530 (NC_000006.11:154474037:TTT: 22/16750)...	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 38667528 (NC_000006.11:154474037:T: 7753/16750) Row 38667529 (NC_000006.11:154474037:TT: 8259/16750) Row 38667530 (NC_000006.11:154474037:TTT: 22/16750)...	-	Apr 26, 2021 (155)
69	14KJPN Submission ignored due to conflicting rows: Row 53636604 (NC_000006.12:154152902:T: 13214/28254) Row 53636605 (NC_000006.12:154152902:TT: 13925/28254) Row 53636606 (NC_000006.12:154152902:TTT: 47/28254)...	-	Oct 14, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 53636604 (NC_000006.12:154152902:T: 13214/28254) Row 53636605 (NC_000006.12:154152902:TT: 13925/28254) Row 53636606 (NC_000006.12:154152902:TTT: 47/28254)...	-	Oct 14, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 53636604 (NC_000006.12:154152902:T: 13214/28254) Row 53636605 (NC_000006.12:154152902:TT: 13925/28254) Row 53636606 (NC_000006.12:154152902:TTT: 47/28254)...	-	Oct 14, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 53636604 (NC_000006.12:154152902:T: 13214/28254) Row 53636605 (NC_000006.12:154152902:TT: 13925/28254) Row 53636606 (NC_000006.12:154152902:TTT: 47/28254)...	-	Oct 14, 2022 (156)
73	UK 10K study - Twins Submission ignored due to conflicting rows: Row 19438333 (NC_000006.11:154474037:TTT: 260/3708) Row 19438334 (NC_000006.11:154474038:T: 2744/3708)	-	Oct 12, 2018 (152)
74	UK 10K study - Twins Submission ignored due to conflicting rows: Row 19438333 (NC_000006.11:154474037:TTT: 260/3708) Row 19438334 (NC_000006.11:154474038:T: 2744/3708)	-	Oct 12, 2018 (152)
75	ALFA	NC_000006.12 - 154152903	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)
rs75300593	Oct 26, 2010 (133)
rs66574007	May 11, 2012 (137)
rs111511657	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4154400990	NC_000006.12:154152902:TTTT:	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
2260646794	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss1705432597, ss1705432673, ss1804749693, ss5180698223, ss5843226433	NC_000006.11:154474037:TTT:	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3718616159, ss4154400989, ss5270956793, ss5719799502	NC_000006.12:154152902:TTT:	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
2260646794	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss103741789	NT_025741.15:58643508:TTT:	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss288810921, ss295315046	NC_000006.10:154515729:TT:	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss666379757, ss1804749692, ss3000223700, ss3734134142, ss3785665487, ss3790985558, ss3795864943, ss3830279683, ss5180698222, ss5843226432	NC_000006.11:154474037:TT:	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss1710301947, ss1710301949	NC_000006.11:154474038:TT:	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3645996336, ss3648505423, ss4154400988, ss5270956790, ss5468347025, ss5719799501	NC_000006.12:154152902:TT:	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
2260646794	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3718616160	NC_000006.12:154152903:TT:	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss42791262, ss95446324	NT_025741.15:58643509:TT:	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss193894629	NT_025741.16:93922968:TT:	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss80905164	NC_000006.9:154566166:T:	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3734134143, ss3790985559, ss5180698221	NC_000006.11:154474037:T:	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
	NC_000006.11:154474038:T:	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4154400987, ss5270956791, ss5468347026, ss5719799500	NC_000006.12:154152902:T:	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
2260646794	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3718616161	NC_000006.12:154152904:T:	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3734134144, ss5180698224	NC_000006.11:154474037::T	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4154400984, ss5270956792, ss5468347027, ss5719799503	NC_000006.12:154152902::T	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
2260646794	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3718616162	NC_000006.12:154152905::T	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4154400985	NC_000006.12:154152902::TT	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
2260646794	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3718616163	NC_000006.12:154152905::TTTTTTTTTT	NC_000006.12:154152902:TTTTTTTTTTT… NC_000006.12:154152902: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 rs34724351

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

rs34724351