Name: rs4927134
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.

rs4927134

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:54518434 (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: A>C
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.195988 (51876/264690, TOPMED)
C=0.135148 (27414/202844, ALFA)
C=0.178262 (24952/139974, GnomAD) (+ 20 more)
C=0.26407 (20782/78700, PAGE_STUDY)
C=0.30529 (8627/28258, 14KJPN)
C=0.30567 (5123/16760, 8.3KJPN)
C=0.2153 (1379/6404, 1000G_30x)
C=0.2153 (1078/5008, 1000G)
C=0.1500 (672/4480, Estonian)
C=0.1201 (463/3854, ALSPAC)
C=0.1146 (425/3708, TWINSUK)
C=0.3427 (1004/2930, KOREAN)
C=0.2318 (483/2084, HGDP_Stanford)
C=0.2230 (422/1892, HapMap)
C=0.3166 (580/1832, Korea1K)
C=0.106 (106/998, GoNL)
C=0.158 (95/600, NorthernSweden)
C=0.190 (41/216, Qatari)
C=0.306 (66/216, Vietnamese)
A=0.404 (84/208, SGDP_PRJ)
C=0.11 (8/74, Ancient Sardinia)
C=0.05 (2/40, GENOME_DK)
A=0.44 (7/16, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LINC02784 : 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	202844	A=0.864852	C=0.135148	0.751868	0.022165	0.225967	32
European	Sub	174928	A=0.879419	C=0.120581	0.774319	0.015481	0.210201	4
African	Sub	7526	A=0.7624	C=0.2376	0.585171	0.060324	0.354504	1
African Others	Sub	264	A=0.761	C=0.239	0.606061	0.083333	0.310606	2
African American	Sub	7262	A=0.7625	C=0.2375	0.584412	0.059488	0.3561	1
Asian	Sub	736	A=0.716	C=0.284	0.513587	0.081522	0.404891	0
East Asian	Sub	590	A=0.686	C=0.314	0.467797	0.094915	0.437288	0
Other Asian	Sub	146	A=0.836	C=0.164	0.69863	0.027397	0.273973	0
Latin American 1	Sub	842	A=0.800	C=0.200	0.638955	0.038005	0.32304	0
Latin American 2	Sub	6876	A=0.6273	C=0.3727	0.394124	0.139616	0.466259	0
South Asian	Sub	5046	A=0.9031	C=0.0969	0.818866	0.012683	0.16845	2
Other	Sub	6890	A=0.8398	C=0.1602	0.711176	0.03164	0.257184	4

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
TopMed	Global	Study-wide	264690	A=0.804012	C=0.195988
Allele Frequency Aggregator	Total	Global	202844	A=0.864852	C=0.135148
Allele Frequency Aggregator	European	Sub	174928	A=0.879419	C=0.120581
Allele Frequency Aggregator	African	Sub	7526	A=0.7624	C=0.2376
Allele Frequency Aggregator	Other	Sub	6890	A=0.8398	C=0.1602
Allele Frequency Aggregator	Latin American 2	Sub	6876	A=0.6273	C=0.3727
Allele Frequency Aggregator	South Asian	Sub	5046	A=0.9031	C=0.0969
Allele Frequency Aggregator	Latin American 1	Sub	842	A=0.800	C=0.200
Allele Frequency Aggregator	Asian	Sub	736	A=0.716	C=0.284
gnomAD - Genomes	Global	Study-wide	139974	A=0.821738	C=0.178262
gnomAD - Genomes	European	Sub	75836	A=0.87100	C=0.12900
gnomAD - Genomes	African	Sub	41916	A=0.76560	C=0.23440
gnomAD - Genomes	American	Sub	13632	A=0.74472	C=0.25528
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	A=0.8612	C=0.1388
gnomAD - Genomes	East Asian	Sub	3124	A=0.6738	C=0.3262
gnomAD - Genomes	Other	Sub	2144	A=0.8209	C=0.1791
The PAGE Study	Global	Study-wide	78700	A=0.73593	C=0.26407
The PAGE Study	AfricanAmerican	Sub	32516	A=0.76412	C=0.23588
The PAGE Study	Mexican	Sub	10810	A=0.63728	C=0.36272
The PAGE Study	Asian	Sub	8318	A=0.6918	C=0.3082
The PAGE Study	PuertoRican	Sub	7918	A=0.7517	C=0.2483
The PAGE Study	NativeHawaiian	Sub	4534	A=0.7256	C=0.2744
The PAGE Study	Cuban	Sub	4230	A=0.8234	C=0.1766
The PAGE Study	Dominican	Sub	3828	A=0.7861	C=0.2139
The PAGE Study	CentralAmerican	Sub	2450	A=0.6747	C=0.3253
The PAGE Study	SouthAmerican	Sub	1980	A=0.6364	C=0.3636
The PAGE Study	NativeAmerican	Sub	1260	A=0.7921	C=0.2079
The PAGE Study	SouthAsian	Sub	856	A=0.916	C=0.084
14KJPN	JAPANESE	Study-wide	28258	A=0.69471	C=0.30529
8.3KJPN	JAPANESE	Study-wide	16760	A=0.69433	C=0.30567
1000Genomes_30x	Global	Study-wide	6404	A=0.7847	C=0.2153
1000Genomes_30x	African	Sub	1786	A=0.7699	C=0.2301
1000Genomes_30x	Europe	Sub	1266	A=0.8523	C=0.1477
1000Genomes_30x	South Asian	Sub	1202	A=0.9260	C=0.0740
1000Genomes_30x	East Asian	Sub	1170	A=0.6923	C=0.3077
1000Genomes_30x	American	Sub	980	A=0.661	C=0.339
1000Genomes	Global	Study-wide	5008	A=0.7847	C=0.2153
1000Genomes	African	Sub	1322	A=0.7632	C=0.2368
1000Genomes	East Asian	Sub	1008	A=0.6974	C=0.3026
1000Genomes	Europe	Sub	1006	A=0.8509	C=0.1491
1000Genomes	South Asian	Sub	978	A=0.924	C=0.076
1000Genomes	American	Sub	694	A=0.660	C=0.340
Genetic variation in the Estonian population	Estonian	Study-wide	4480	A=0.8500	C=0.1500
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.8799	C=0.1201
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.8854	C=0.1146
KOREAN population from KRGDB	KOREAN	Study-wide	2930	A=0.6573	C=0.3427
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	A=0.7682	C=0.2318
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	A=0.681	C=0.319
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	A=0.901	C=0.099
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	A=0.826	C=0.174
HGDP-CEPH-db Supplement 1	Europe	Sub	320	A=0.866	C=0.134
HGDP-CEPH-db Supplement 1	Africa	Sub	242	A=0.752	C=0.248
HGDP-CEPH-db Supplement 1	America	Sub	216	A=0.495	C=0.505
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	A=0.74	C=0.26
HapMap	Global	Study-wide	1892	A=0.7770	C=0.2230
HapMap	American	Sub	770	A=0.778	C=0.222
HapMap	African	Sub	692	A=0.799	C=0.201
HapMap	Asian	Sub	254	A=0.661	C=0.339
HapMap	Europe	Sub	176	A=0.852	C=0.148
Korean Genome Project	KOREAN	Study-wide	1832	A=0.6834	C=0.3166
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	A=0.894	C=0.106
Northern Sweden	ACPOP	Study-wide	600	A=0.842	C=0.158
Qatari	Global	Study-wide	216	A=0.810	C=0.190
A Vietnamese Genetic Variation Database	Global	Study-wide	216	A=0.694	C=0.306
SGDP_PRJ	Global	Study-wide	208	A=0.404	C=0.596
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	74	A=0.89	C=0.11
The Danish reference pan genome	Danish	Study-wide	40	A=0.95	C=0.05
Siberian	Global	Study-wide	16	A=0.44	C=0.56

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 1	NC_000001.11:g.54518434A>C
GRCh37.p13 chr 1	NC_000001.10:g.54984107A>C

Gene: LINC02784, uncharacterized LINC02784 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LINC02784 transcript variant X1	XR_007066097.1:n.	N/A	Intron Variant
LINC02784 transcript variant X3	XR_007066098.1:n.	N/A	Intron Variant
LINC02784 transcript variant X2	XR_947372.2: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	A=	C
GRCh38.p14 chr 1	NC_000001.11:g.54518434=	NC_000001.11:g.54518434A>C
GRCh37.p13 chr 1	NC_000001.10:g.54984107=	NC_000001.10:g.54984107A>C

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#.

114 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	WI_SSAHASNP	ss6812594	Feb 20, 2003 (111)
2	ILLUMINA	ss66685455	Nov 30, 2006 (127)
3	ILLUMINA	ss67399914	Nov 30, 2006 (127)
4	ILLUMINA	ss67769699	Nov 30, 2006 (127)
5	ILLUMINA	ss70836673	May 26, 2008 (130)
6	ILLUMINA	ss71420001	May 17, 2007 (127)
7	ILLUMINA	ss75558610	Dec 07, 2007 (129)
8	ILLUMINA	ss79202893	Dec 16, 2007 (130)
9	KRIBB_YJKIM	ss84400951	Dec 16, 2007 (130)
10	BGI	ss102741772	Dec 01, 2009 (131)
11	1000GENOMES	ss108200393	Jan 23, 2009 (130)
12	1000GENOMES	ss110450518	Jan 24, 2009 (130)
13	ILLUMINA	ss122433311	Dec 01, 2009 (131)
14	ILLUMINA	ss154329625	Dec 01, 2009 (131)
15	ILLUMINA	ss159506139	Dec 01, 2009 (131)
16	ILLUMINA	ss160728907	Dec 01, 2009 (131)
17	COMPLETE_GENOMICS	ss163389545	Jul 04, 2010 (132)
18	ILLUMINA	ss171980896	Jul 04, 2010 (132)
19	ILLUMINA	ss173877977	Jul 04, 2010 (132)
20	BUSHMAN	ss198452037	Jul 04, 2010 (132)
21	1000GENOMES	ss218382667	Jul 14, 2010 (132)
22	1000GENOMES	ss230532745	Jul 14, 2010 (132)
23	1000GENOMES	ss238227362	Jul 15, 2010 (132)
24	GMI	ss275824830	May 04, 2012 (137)
25	GMI	ss284049262	Apr 25, 2013 (138)
26	PJP	ss290510478	May 09, 2011 (134)
27	ILLUMINA	ss481103682	May 04, 2012 (137)
28	ILLUMINA	ss481125662	May 04, 2012 (137)
29	ILLUMINA	ss482116369	Sep 08, 2015 (146)
30	ILLUMINA	ss485346919	May 04, 2012 (137)
31	ILLUMINA	ss537294586	Sep 08, 2015 (146)
32	TISHKOFF	ss554107754	Apr 25, 2013 (138)
33	SSMP	ss647936490	Apr 25, 2013 (138)
34	ILLUMINA	ss778925186	Sep 08, 2015 (146)
35	ILLUMINA	ss783119194	Sep 08, 2015 (146)
36	ILLUMINA	ss784076000	Sep 08, 2015 (146)
37	ILLUMINA	ss825533411	Apr 01, 2015 (144)
38	ILLUMINA	ss832377947	Sep 08, 2015 (146)
39	ILLUMINA	ss833017479	Jul 12, 2019 (153)
40	ILLUMINA	ss834386658	Sep 08, 2015 (146)
41	EVA-GONL	ss975156376	Aug 21, 2014 (142)
42	JMKIDD_LAB	ss1067882987	Aug 21, 2014 (142)
43	1000GENOMES	ss1290879274	Aug 21, 2014 (142)
44	EVA_GENOME_DK	ss1574055887	Apr 01, 2015 (144)
45	EVA_DECODE	ss1584522619	Apr 01, 2015 (144)
46	EVA_UK10K_ALSPAC	ss1600166092	Apr 01, 2015 (144)
47	EVA_UK10K_TWINSUK	ss1643160125	Apr 01, 2015 (144)
48	EVA_SVP	ss1712332516	Apr 01, 2015 (144)
49	ILLUMINA	ss1751924869	Sep 08, 2015 (146)
50	HAMMER_LAB	ss1794355846	Sep 08, 2015 (146)
51	WEILL_CORNELL_DGM	ss1918365150	Feb 12, 2016 (147)
52	ILLUMINA	ss1958272766	Feb 12, 2016 (147)
53	GENOMED	ss1966744096	Jul 19, 2016 (147)
54	JJLAB	ss2019697804	Sep 14, 2016 (149)
55	ILLUMINA	ss2094958634	Dec 20, 2016 (150)
56	USC_VALOUEV	ss2147711966	Dec 20, 2016 (150)
57	HUMAN_LONGEVITY	ss2162478669	Dec 20, 2016 (150)
58	SYSTEMSBIOZJU	ss2624361678	Nov 08, 2017 (151)
59	ILLUMINA	ss2632514708	Nov 08, 2017 (151)
60	GRF	ss2697623908	Nov 08, 2017 (151)
61	GNOMAD	ss2755117407	Nov 08, 2017 (151)
62	SWEGEN	ss2986811757	Nov 08, 2017 (151)
63	ILLUMINA	ss3021087571	Nov 08, 2017 (151)
64	BIOINF_KMB_FNS_UNIBA	ss3023608900	Nov 08, 2017 (151)
65	CSHL	ss3343451704	Nov 08, 2017 (151)
66	ILLUMINA	ss3626096683	Oct 11, 2018 (152)
67	ILLUMINA	ss3630550956	Oct 11, 2018 (152)
68	ILLUMINA	ss3632891209	Oct 11, 2018 (152)
69	ILLUMINA	ss3633585798	Oct 11, 2018 (152)
70	ILLUMINA	ss3634324252	Oct 11, 2018 (152)
71	ILLUMINA	ss3635279687	Oct 11, 2018 (152)
72	ILLUMINA	ss3635999748	Oct 11, 2018 (152)
73	ILLUMINA	ss3637030103	Oct 11, 2018 (152)
74	ILLUMINA	ss3637756495	Oct 11, 2018 (152)
75	ILLUMINA	ss3638897145	Oct 11, 2018 (152)
76	ILLUMINA	ss3639446024	Oct 11, 2018 (152)
77	ILLUMINA	ss3640031613	Oct 11, 2018 (152)
78	ILLUMINA	ss3642768719	Oct 11, 2018 (152)
79	ILLUMINA	ss3651413941	Oct 11, 2018 (152)
80	EGCUT_WGS	ss3654875526	Jul 12, 2019 (153)
81	EVA_DECODE	ss3686765003	Jul 12, 2019 (153)
82	ILLUMINA	ss3725024448	Jul 12, 2019 (153)
83	ACPOP	ss3727043503	Jul 12, 2019 (153)
84	ILLUMINA	ss3744625176	Jul 12, 2019 (153)
85	EVA	ss3746199104	Jul 12, 2019 (153)
86	PAGE_CC	ss3770808693	Jul 12, 2019 (153)
87	ILLUMINA	ss3772126603	Jul 12, 2019 (153)
88	KHV_HUMAN_GENOMES	ss3799208169	Jul 12, 2019 (153)
89	EVA	ss3826169335	Apr 25, 2020 (154)
90	HGDP	ss3847333048	Apr 25, 2020 (154)
91	SGDP_PRJ	ss3848839050	Apr 25, 2020 (154)
92	KRGDB	ss3893848972	Apr 25, 2020 (154)
93	KOGIC	ss3944505089	Apr 25, 2020 (154)
94	EVA	ss3984795773	Apr 25, 2021 (155)
95	EVA	ss4016910067	Apr 25, 2021 (155)
96	TOPMED	ss4449638807	Apr 25, 2021 (155)
97	TOMMO_GENOMICS	ss5143936702	Apr 25, 2021 (155)
98	1000G_HIGH_COVERAGE	ss5242257939	Oct 12, 2022 (156)
99	EVA	ss5314614911	Oct 12, 2022 (156)
100	EVA	ss5318703624	Oct 12, 2022 (156)
101	HUGCELL_USP	ss5443320783	Oct 12, 2022 (156)
102	1000G_HIGH_COVERAGE	ss5514528734	Oct 12, 2022 (156)
103	SANFORD_IMAGENETICS	ss5624204794	Oct 12, 2022 (156)
104	SANFORD_IMAGENETICS	ss5625521854	Oct 12, 2022 (156)
105	TOMMO_GENOMICS	ss5668706063	Oct 12, 2022 (156)
106	EVA	ss5799483719	Oct 12, 2022 (156)
107	YY_MCH	ss5800592350	Oct 12, 2022 (156)
108	EVA	ss5831954174	Oct 12, 2022 (156)
109	EVA	ss5847158233	Oct 12, 2022 (156)
110	EVA	ss5847538701	Oct 12, 2022 (156)
111	EVA	ss5848903241	Oct 12, 2022 (156)
112	EVA	ss5908245998	Oct 12, 2022 (156)
113	EVA	ss5937353185	Oct 12, 2022 (156)
114	EVA	ss5979273789	Oct 12, 2022 (156)
115	1000Genomes	NC_000001.10 - 54984107	Oct 11, 2018 (152)
116	1000Genomes_30x	NC_000001.11 - 54518434	Oct 12, 2022 (156)
117	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 54984107	Oct 11, 2018 (152)
118	Genetic variation in the Estonian population	NC_000001.10 - 54984107	Oct 11, 2018 (152)
119	The Danish reference pan genome	NC_000001.10 - 54984107	Apr 25, 2020 (154)
120	gnomAD - Genomes	NC_000001.11 - 54518434	Apr 25, 2021 (155)
121	Genome of the Netherlands Release 5	NC_000001.10 - 54984107	Apr 25, 2020 (154)
122	HGDP-CEPH-db Supplement 1	NC_000001.9 - 54756695	Apr 25, 2020 (154)
123	HapMap	NC_000001.11 - 54518434	Apr 25, 2020 (154)
124	KOREAN population from KRGDB	NC_000001.10 - 54984107	Apr 25, 2020 (154)
125	Korean Genome Project	NC_000001.11 - 54518434	Apr 25, 2020 (154)
126	Northern Sweden	NC_000001.10 - 54984107	Jul 12, 2019 (153)
127	The PAGE Study	NC_000001.11 - 54518434	Jul 12, 2019 (153)
128	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000001.10 - 54984107	Apr 25, 2021 (155)
129	Qatari	NC_000001.10 - 54984107	Apr 25, 2020 (154)
130	SGDP_PRJ	NC_000001.10 - 54984107	Apr 25, 2020 (154)
131	Siberian	NC_000001.10 - 54984107	Apr 25, 2020 (154)
132	8.3KJPN	NC_000001.10 - 54984107	Apr 25, 2021 (155)
133	14KJPN	NC_000001.11 - 54518434	Oct 12, 2022 (156)
134	TopMed	NC_000001.11 - 54518434	Apr 25, 2021 (155)
135	UK 10K study - Twins	NC_000001.10 - 54984107	Oct 11, 2018 (152)
136	A Vietnamese Genetic Variation Database	NC_000001.10 - 54984107	Jul 12, 2019 (153)
137	ALFA	NC_000001.11 - 54518434	Apr 25, 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)
rs61178272	May 26, 2008 (130)
rs117876241	Aug 16, 2010 (132)
rs386596483	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3638897145, ss3639446024	NC_000001.8:54696127:A:C	NC_000001.11:54518433:A:C	(self)
10940, ss108200393, ss110450518, ss163389545, ss198452037, ss275824830, ss284049262, ss290510478, ss481103682, ss825533411, ss1584522619, ss1712332516, ss3642768719, ss3847333048	NC_000001.9:54756694:A:C	NC_000001.11:54518433:A:C	(self)
1597172, 868344, 613774, 1499825, 367935, 1026366, 328368, 21700, 407080, 856030, 228320, 1906009, 868344, 177766, ss218382667, ss230532745, ss238227362, ss481125662, ss482116369, ss485346919, ss537294586, ss554107754, ss647936490, ss778925186, ss783119194, ss784076000, ss832377947, ss833017479, ss834386658, ss975156376, ss1067882987, ss1290879274, ss1574055887, ss1600166092, ss1643160125, ss1751924869, ss1794355846, ss1918365150, ss1958272766, ss1966744096, ss2019697804, ss2094958634, ss2147711966, ss2624361678, ss2632514708, ss2697623908, ss2755117407, ss2986811757, ss3021087571, ss3343451704, ss3626096683, ss3630550956, ss3632891209, ss3633585798, ss3634324252, ss3635279687, ss3635999748, ss3637030103, ss3637756495, ss3640031613, ss3651413941, ss3654875526, ss3727043503, ss3744625176, ss3746199104, ss3772126603, ss3826169335, ss3848839050, ss3893848972, ss3984795773, ss4016910067, ss5143936702, ss5314614911, ss5318703624, ss5624204794, ss5625521854, ss5799483719, ss5831954174, ss5847158233, ss5847538701, ss5937353185, ss5979273789	NC_000001.10:54984106:A:C	NC_000001.11:54518433:A:C	(self)
2054669, 11313894, 67353, 883090, 30162, 2543167, 13245142, 9935963913, ss2162478669, ss3023608900, ss3686765003, ss3725024448, ss3770808693, ss3799208169, ss3944505089, ss4449638807, ss5242257939, ss5443320783, ss5514528734, ss5668706063, ss5800592350, ss5848903241, ss5908245998	NC_000001.11:54518433:A:C	NC_000001.11:54518433:A:C	(self)
ss6812594, ss66685455, ss67399914, ss67769699, ss70836673, ss71420001, ss75558610, ss79202893, ss84400951, ss102741772, ss122433311, ss154329625, ss159506139, ss160728907, ss171980896, ss173877977	NT_032977.9:24956024:A:C	NC_000001.11:54518433:A:C	(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 rs4927134

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

rs4927134