Name: rs4348534
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.

rs4348534

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr8:134260026 (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: C>A / C>G / C>T
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.460456 (121878/264690, TOPMED)
C=0.470196 (95351/202790, ALFA)
C=0.458644 (64179/139932, GnomAD) (+ 19 more)
C=0.23416 (6617/28258, 14KJPN)
C=0.23461 (3932/16760, 8.3KJPN)
C=0.4062 (2601/6404, 1000G_30x)
C=0.3990 (1998/5008, 1000G)
C=0.4096 (1835/4480, Estonian)
C=0.4725 (1821/3854, ALSPAC)
C=0.4795 (1778/3708, TWINSUK)
C=0.2181 (639/2930, KOREAN)
C=0.4122 (859/2084, HGDP_Stanford)
C=0.2243 (411/1832, Korea1K)
T=0.4533 (515/1136, Daghestan)
C=0.480 (479/998, GoNL)
C=0.450 (270/600, NorthernSweden)
C=0.245 (112/458, SGDP_PRJ)
T=0.352 (76/216, Qatari)
C=0.248 (53/214, Vietnamese)
C=0.35 (17/48, Siberian)
T=0.48 (22/46, Ancient Sardinia)
T=0.38 (15/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: None
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20230706150541

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	202790	C=0.470196	T=0.529804
European	Sub	172842	C=0.473826	T=0.526174
African	Sub	9732	C=0.4642	T=0.5358
African Others	Sub	348	C=0.486	T=0.514
African American	Sub	9384	C=0.4634	T=0.5366
Asian	Sub	704	C=0.246	T=0.754
East Asian	Sub	558	C=0.224	T=0.776
Other Asian	Sub	146	C=0.329	T=0.671
Latin American 1	Sub	844	C=0.412	T=0.588
Latin American 2	Sub	6910	C=0.4334	T=0.5666
South Asian	Sub	5044	C=0.4411	T=0.5589
Other	Sub	6714	C=0.4759	T=0.5241

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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	C=0.460456	T=0.539544
Allele Frequency Aggregator	Total	Global	202790	C=0.470196	T=0.529804
Allele Frequency Aggregator	European	Sub	172842	C=0.473826	T=0.526174
Allele Frequency Aggregator	African	Sub	9732	C=0.4642	T=0.5358
Allele Frequency Aggregator	Latin American 2	Sub	6910	C=0.4334	T=0.5666
Allele Frequency Aggregator	Other	Sub	6714	C=0.4759	T=0.5241
Allele Frequency Aggregator	South Asian	Sub	5044	C=0.4411	T=0.5589
Allele Frequency Aggregator	Latin American 1	Sub	844	C=0.412	T=0.588
Allele Frequency Aggregator	Asian	Sub	704	C=0.246	T=0.754
gnomAD - Genomes	Global	Study-wide	139932	C=0.458644	T=0.541356
gnomAD - Genomes	European	Sub	75794	C=0.45996	T=0.54004
gnomAD - Genomes	African	Sub	41914	C=0.46521	T=0.53479
gnomAD - Genomes	American	Sub	13636	C=0.46363	T=0.53637
gnomAD - Genomes	Ashkenazi Jewish	Sub	3320	C=0.5166	T=0.4834
gnomAD - Genomes	East Asian	Sub	3116	C=0.2478	T=0.7522
gnomAD - Genomes	Other	Sub	2152	C=0.4689	T=0.5311
14KJPN	JAPANESE	Study-wide	28258	C=0.23416	T=0.76584
8.3KJPN	JAPANESE	Study-wide	16760	C=0.23461	T=0.76539
1000Genomes_30x	Global	Study-wide	6404	C=0.4062	T=0.5938
1000Genomes_30x	African	Sub	1786	C=0.4770	T=0.5230
1000Genomes_30x	Europe	Sub	1266	C=0.4502	T=0.5498
1000Genomes_30x	South Asian	Sub	1202	C=0.3935	T=0.6065
1000Genomes_30x	East Asian	Sub	1170	C=0.2530	T=0.7470
1000Genomes_30x	American	Sub	980	C=0.418	T=0.582
1000Genomes	Global	Study-wide	5008	C=0.3990	T=0.6010
1000Genomes	African	Sub	1322	C=0.4720	T=0.5280
1000Genomes	East Asian	Sub	1008	C=0.2450	T=0.7550
1000Genomes	Europe	Sub	1006	C=0.4453	T=0.5547
1000Genomes	South Asian	Sub	978	C=0.399	T=0.601
1000Genomes	American	Sub	694	C=0.416	T=0.584
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.4096	T=0.5904
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.4725	T=0.5275
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.4795	T=0.5205
KOREAN population from KRGDB	KOREAN	Study-wide	2930	C=0.2181	A=0.0000, G=0.0000, T=0.7819
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	C=0.4122	T=0.5878
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	C=0.194	T=0.806
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	C=0.486	T=0.514
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	C=0.586	T=0.414
HGDP-CEPH-db Supplement 1	Europe	Sub	320	C=0.544	T=0.456
HGDP-CEPH-db Supplement 1	Africa	Sub	242	C=0.450	T=0.550
HGDP-CEPH-db Supplement 1	America	Sub	216	C=0.347	T=0.653
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	C=0.06	T=0.94
Korean Genome Project	KOREAN	Study-wide	1832	C=0.2243	T=0.7757
Genome-wide autozygosity in Daghestan	Global	Study-wide	1136	C=0.5467	T=0.4533
Genome-wide autozygosity in Daghestan	Daghestan	Sub	628	C=0.599	T=0.401
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	C=0.521	T=0.479
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	C=0.443	T=0.557
Genome-wide autozygosity in Daghestan	Europe	Sub	108	C=0.528	T=0.472
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	C=0.36	T=0.64
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	C=0.67	T=0.33
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.480	T=0.520
Northern Sweden	ACPOP	Study-wide	600	C=0.450	T=0.550
SGDP_PRJ	Global	Study-wide	458	C=0.245	T=0.755
Qatari	Global	Study-wide	216	C=0.648	T=0.352
A Vietnamese Genetic Variation Database	Global	Study-wide	214	C=0.248	T=0.752
Siberian	Global	Study-wide	48	C=0.35	T=0.65
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	46	C=0.52	T=0.48
The Danish reference pan genome	Danish	Study-wide	40	C=0.62	T=0.38

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 8	NC_000008.11:g.134260026C>A
GRCh38.p14 chr 8	NC_000008.11:g.134260026C>G
GRCh38.p14 chr 8	NC_000008.11:g.134260026C>T
GRCh37.p13 chr 8	NC_000008.10:g.135272269C>A
GRCh37.p13 chr 8	NC_000008.10:g.135272269C>G
GRCh37.p13 chr 8	NC_000008.10:g.135272269C>T

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	C=	A	G	T
GRCh38.p14 chr 8	NC_000008.11:g.134260026=	NC_000008.11:g.134260026C>A	NC_000008.11:g.134260026C>G	NC_000008.11:g.134260026C>T
GRCh37.p13 chr 8	NC_000008.10:g.135272269=	NC_000008.10:g.135272269C>A	NC_000008.10:g.135272269C>G	NC_000008.10:g.135272269C>T

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#.

124 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SC_JCM	ss5785824	Feb 20, 2003 (111)
2	WI_SSAHASNP	ss11965898	Jul 11, 2003 (116)
3	ABI	ss44924795	Mar 13, 2006 (126)
4	ILLUMINA	ss66747858	Dec 02, 2006 (127)
5	ILLUMINA	ss67328905	Dec 02, 2006 (127)
6	ILLUMINA	ss67729612	Dec 02, 2006 (127)
7	ILLUMINA	ss70800941	May 25, 2008 (130)
8	ILLUMINA	ss71379764	May 18, 2007 (127)
9	ILLUMINA	ss75709591	Dec 07, 2007 (129)
10	ILLUMINA	ss79180042	Dec 15, 2007 (130)
11	KRIBB_YJKIM	ss84254863	Dec 15, 2007 (130)
12	HGSV	ss86127992	Dec 15, 2007 (130)
13	BCMHGSC_JDW	ss93975038	Mar 25, 2008 (129)
14	HUMANGENOME_JCVI	ss97905711	Feb 05, 2009 (130)
15	BGI	ss105648061	Feb 05, 2009 (130)
16	1000GENOMES	ss108433803	Jan 23, 2009 (130)
17	1000GENOMES	ss113845899	Jan 25, 2009 (130)
18	ILLUMINA	ss122298361	Dec 01, 2009 (131)
19	ENSEMBL	ss134511359	Dec 01, 2009 (131)
20	ENSEMBL	ss143814981	Dec 01, 2009 (131)
21	ILLUMINA	ss154291014	Dec 01, 2009 (131)
22	GMI	ss156942332	Dec 01, 2009 (131)
23	ILLUMINA	ss159467979	Dec 01, 2009 (131)
24	ILLUMINA	ss160674153	Dec 01, 2009 (131)
25	COMPLETE_GENOMICS	ss162837305	Jul 04, 2010 (132)
26	COMPLETE_GENOMICS	ss165805746	Jul 04, 2010 (132)
27	COMPLETE_GENOMICS	ss167188004	Jul 04, 2010 (132)
28	ILLUMINA	ss171779797	Jul 04, 2010 (132)
29	ILLUMINA	ss173719120	Jul 04, 2010 (132)
30	BUSHMAN	ss199839640	Jul 04, 2010 (132)
31	BCM-HGSC-SUB	ss208544194	Jul 04, 2010 (132)
32	1000GENOMES	ss224010075	Jul 14, 2010 (132)
33	1000GENOMES	ss234649990	Jul 15, 2010 (132)
34	1000GENOMES	ss241458524	Jul 15, 2010 (132)
35	BL	ss254688810	May 09, 2011 (134)
36	GMI	ss280025559	May 04, 2012 (137)
37	GMI	ss285934770	Apr 25, 2013 (138)
38	PJP	ss294193744	May 09, 2011 (134)
39	ILLUMINA	ss480929068	May 04, 2012 (137)
40	ILLUMINA	ss480948517	May 04, 2012 (137)
41	ILLUMINA	ss481911169	Sep 08, 2015 (146)
42	ILLUMINA	ss485259542	May 04, 2012 (137)
43	ILLUMINA	ss537229426	Sep 08, 2015 (146)
44	TISHKOFF	ss561104996	Apr 25, 2013 (138)
45	SSMP	ss655538649	Apr 25, 2013 (138)
46	ILLUMINA	ss778906481	Sep 08, 2015 (146)
47	ILLUMINA	ss783075717	Sep 08, 2015 (146)
48	ILLUMINA	ss784033440	Sep 08, 2015 (146)
49	ILLUMINA	ss825510560	Apr 01, 2015 (144)
50	ILLUMINA	ss832333934	Sep 08, 2015 (146)
51	ILLUMINA	ss832979464	Jul 13, 2019 (153)
52	ILLUMINA	ss834367790	Sep 08, 2015 (146)
53	EVA-GONL	ss986112480	Aug 21, 2014 (142)
54	JMKIDD_LAB	ss1075959158	Aug 21, 2014 (142)
55	1000GENOMES	ss1332119950	Aug 21, 2014 (142)
56	HAMMER_LAB	ss1397541535	Sep 08, 2015 (146)
57	DDI	ss1431687980	Apr 01, 2015 (144)
58	EVA_GENOME_DK	ss1582908472	Apr 01, 2015 (144)
59	EVA_DECODE	ss1595731229	Apr 01, 2015 (144)
60	EVA_UK10K_ALSPAC	ss1621846500	Apr 01, 2015 (144)
61	EVA_UK10K_TWINSUK	ss1664840533	Apr 01, 2015 (144)
62	EVA_SVP	ss1713075441	Apr 01, 2015 (144)
63	ILLUMINA	ss1752715024	Sep 08, 2015 (146)
64	HAMMER_LAB	ss1805786587	Sep 08, 2015 (146)
65	WEILL_CORNELL_DGM	ss1929386820	Feb 12, 2016 (147)
66	GENOMED	ss1971105911	Jul 19, 2016 (147)
67	JJLAB	ss2025397492	Sep 14, 2016 (149)
68	USC_VALOUEV	ss2153626801	Dec 20, 2016 (150)
69	HUMAN_LONGEVITY	ss2307806453	Dec 20, 2016 (150)
70	SYSTEMSBIOZJU	ss2627173244	Nov 08, 2017 (151)
71	ILLUMINA	ss2634811028	Nov 08, 2017 (151)
72	GRF	ss2709415011	Nov 08, 2017 (151)
73	GNOMAD	ss2873269598	Nov 08, 2017 (151)
74	SWEGEN	ss3004080379	Nov 08, 2017 (151)
75	BIOINF_KMB_FNS_UNIBA	ss3026485530	Nov 08, 2017 (151)
76	CSHL	ss3348430727	Nov 08, 2017 (151)
77	ILLUMINA	ss3630170702	Oct 12, 2018 (152)
78	ILLUMINA	ss3632706816	Oct 12, 2018 (152)
79	ILLUMINA	ss3633518006	Oct 12, 2018 (152)
80	ILLUMINA	ss3634245464	Oct 12, 2018 (152)
81	ILLUMINA	ss3635193043	Oct 12, 2018 (152)
82	ILLUMINA	ss3635923843	Oct 12, 2018 (152)
83	ILLUMINA	ss3636936315	Oct 12, 2018 (152)
84	ILLUMINA	ss3637677094	Oct 12, 2018 (152)
85	ILLUMINA	ss3638789294	Oct 12, 2018 (152)
86	ILLUMINA	ss3639397859	Oct 12, 2018 (152)
87	ILLUMINA	ss3639730297	Oct 12, 2018 (152)
88	ILLUMINA	ss3640900334	Oct 12, 2018 (152)
89	ILLUMINA	ss3643718139	Oct 12, 2018 (152)
90	URBANLAB	ss3649027425	Oct 12, 2018 (152)
91	EGCUT_WGS	ss3671808133	Jul 13, 2019 (153)
92	EVA_DECODE	ss3723106754	Jul 13, 2019 (153)
93	ACPOP	ss3736146675	Jul 13, 2019 (153)
94	ILLUMINA	ss3745493029	Jul 13, 2019 (153)
95	EVA	ss3768674153	Jul 13, 2019 (153)
96	ILLUMINA	ss3772985213	Jul 13, 2019 (153)
97	PACBIO	ss3786294772	Jul 13, 2019 (153)
98	PACBIO	ss3791526147	Jul 13, 2019 (153)
99	PACBIO	ss3796407719	Jul 13, 2019 (153)
100	KHV_HUMAN_GENOMES	ss3811838454	Jul 13, 2019 (153)
101	EVA	ss3831441222	Apr 26, 2020 (154)
102	EVA	ss3839230248	Apr 26, 2020 (154)
103	EVA	ss3844690978	Apr 26, 2020 (154)
104	HGDP	ss3847932165	Apr 26, 2020 (154)
105	SGDP_PRJ	ss3871103806	Apr 26, 2020 (154)
106	KRGDB	ss3918711169	Apr 26, 2020 (154)
107	KOGIC	ss3964935704	Apr 26, 2020 (154)
108	EVA	ss3985393131	Apr 26, 2021 (155)
109	EVA	ss4017416884	Apr 26, 2021 (155)
110	TOPMED	ss4805967557	Apr 26, 2021 (155)
111	TOMMO_GENOMICS	ss5191222772	Apr 26, 2021 (155)
112	1000G_HIGH_COVERAGE	ss5279120666	Oct 16, 2022 (156)
113	EVA	ss5315368230	Oct 16, 2022 (156)
114	EVA	ss5384791405	Oct 16, 2022 (156)
115	HUGCELL_USP	ss5475484990	Oct 16, 2022 (156)
116	1000G_HIGH_COVERAGE	ss5570540659	Oct 16, 2022 (156)
117	SANFORD_IMAGENETICS	ss5646517961	Oct 16, 2022 (156)
118	TOMMO_GENOMICS	ss5734010938	Oct 16, 2022 (156)
119	EVA	ss5799770867	Oct 16, 2022 (156)
120	YY_MCH	ss5810177478	Oct 16, 2022 (156)
121	EVA	ss5831294487	Oct 16, 2022 (156)
122	EVA	ss5856592877	Oct 16, 2022 (156)
123	EVA	ss5891238545	Oct 16, 2022 (156)
124	EVA	ss5975777959	Oct 16, 2022 (156)
125	1000Genomes	NC_000008.10 - 135272269	Oct 12, 2018 (152)
126	1000Genomes_30x	NC_000008.11 - 134260026	Oct 16, 2022 (156)
127	The Avon Longitudinal Study of Parents and Children	NC_000008.10 - 135272269	Oct 12, 2018 (152)
128	Genome-wide autozygosity in Daghestan	NC_000008.9 - 135341451	Apr 26, 2020 (154)
129	Genetic variation in the Estonian population	NC_000008.10 - 135272269	Oct 12, 2018 (152)
130	The Danish reference pan genome	NC_000008.10 - 135272269	Apr 26, 2020 (154)
131	gnomAD - Genomes	NC_000008.11 - 134260026	Apr 26, 2021 (155)
132	Genome of the Netherlands Release 5	NC_000008.10 - 135272269	Apr 26, 2020 (154)
133	HGDP-CEPH-db Supplement 1	NC_000008.9 - 135341451	Apr 26, 2020 (154)
134	KOREAN population from KRGDB	NC_000008.10 - 135272269	Apr 26, 2020 (154)
135	Korean Genome Project	NC_000008.11 - 134260026	Apr 26, 2020 (154)
136	Northern Sweden	NC_000008.10 - 135272269	Jul 13, 2019 (153)
137	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000008.10 - 135272269	Apr 26, 2021 (155)
138	Qatari	NC_000008.10 - 135272269	Apr 26, 2020 (154)
139	SGDP_PRJ	NC_000008.10 - 135272269	Apr 26, 2020 (154)
140	Siberian	NC_000008.10 - 135272269	Apr 26, 2020 (154)
141	8.3KJPN	NC_000008.10 - 135272269	Apr 26, 2021 (155)
142	14KJPN	NC_000008.11 - 134260026	Oct 16, 2022 (156)
143	TopMed	NC_000008.11 - 134260026	Apr 26, 2021 (155)
144	UK 10K study - Twins	NC_000008.10 - 135272269	Oct 12, 2018 (152)
145	A Vietnamese Genetic Variation Database	NC_000008.10 - 135272269	Jul 13, 2019 (153)
146	ALFA	NC_000008.11 - 134260026	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)
rs59736034	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
25888563, ss3918711169	NC_000008.10:135272268:C:A	NC_000008.11:134260025:C:A	(self)
25888563, ss3918711169	NC_000008.10:135272268:C:G	NC_000008.11:134260025:C:G	(self)
515147, 610057, ss86127992, ss93975038, ss108433803, ss113845899, ss162837305, ss165805746, ss167188004, ss199839640, ss208544194, ss254688810, ss280025559, ss285934770, ss294193744, ss480929068, ss825510560, ss1397541535, ss1595731229, ss1713075441, ss3639397859, ss3639730297, ss3643718139, ss3847932165	NC_000008.9:135341450:C:T	NC_000008.11:134260025:C:T	(self)
44325972, 24671139, 17546381, 9073409, 11007155, 25888563, 9431540, 619058, 11428750, 23120786, 6143155, 49192079, 24671139, 5479107, ss224010075, ss234649990, ss241458524, ss480948517, ss481911169, ss485259542, ss537229426, ss561104996, ss655538649, ss778906481, ss783075717, ss784033440, ss832333934, ss832979464, ss834367790, ss986112480, ss1075959158, ss1332119950, ss1431687980, ss1582908472, ss1621846500, ss1664840533, ss1752715024, ss1805786587, ss1929386820, ss1971105911, ss2025397492, ss2153626801, ss2627173244, ss2634811028, ss2709415011, ss2873269598, ss3004080379, ss3348430727, ss3630170702, ss3632706816, ss3633518006, ss3634245464, ss3635193043, ss3635923843, ss3636936315, ss3637677094, ss3638789294, ss3640900334, ss3671808133, ss3736146675, ss3745493029, ss3768674153, ss3772985213, ss3786294772, ss3791526147, ss3796407719, ss3831441222, ss3839230248, ss3871103806, ss3918711169, ss3985393131, ss4017416884, ss5191222772, ss5315368230, ss5384791405, ss5646517961, ss5799770867, ss5831294487, ss5975777959	NC_000008.10:135272268:C:T	NC_000008.11:134260025:C:T	(self)
58066594, 312617126, 21313705, 67848042, 643345117, 1757044414, ss2307806453, ss3026485530, ss3649027425, ss3723106754, ss3811838454, ss3844690978, ss3964935704, ss4805967557, ss5279120666, ss5475484990, ss5570540659, ss5734010938, ss5810177478, ss5856592877, ss5891238545	NC_000008.11:134260025:C:T	NC_000008.11:134260025:C:T	(self)
ss11965898	NT_008046.13:48492531:C:T	NC_000008.11:134260025:C:T	(self)
ss5785824, ss44924795, ss66747858, ss67328905, ss67729612, ss70800941, ss71379764, ss75709591, ss79180042, ss84254863, ss97905711, ss105648061, ss122298361, ss134511359, ss143814981, ss154291014, ss156942332, ss159467979, ss160674153, ss171779797, ss173719120	NT_008046.16:48545817:C:T	NC_000008.11:134260025:C:T	(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 rs4348534

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
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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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs4348534