Name: rs4813630
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.

rs4813630

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr20:3174762 (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
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.499486 (132209/264690, TOPMED)
C=0.496246 (69529/140110, GnomAD)
C=0.429707 (49785/115858, ALFA) (+ 19 more)
A=0.47417 (37315/78696, PAGE_STUDY)
C=0.31333 (8854/28258, 14KJPN)
C=0.31098 (5212/16760, 8.3KJPN)
C=0.4482 (2870/6404, 1000G_30x)
C=0.4343 (2175/5008, 1000G)
C=0.4281 (1918/4480, Estonian)
C=0.4598 (1772/3854, ALSPAC)
C=0.4563 (1692/3708, TWINSUK)
C=0.3655 (1071/2930, KOREAN)
C=0.3690 (676/1832, Korea1K)
C=0.461 (460/998, GoNL)
C=0.432 (342/792, PRJEB37584)
C=0.460 (276/600, NorthernSweden)
C=0.258 (112/434, SGDP_PRJ)
C=0.347 (75/216, Qatari)
C=0.368 (78/212, Vietnamese)
C=0.35 (14/40, GENOME_DK)
C=0.25 (9/36, Siberian)
C=0.33 (4/12, Ancient Sardinia)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LZTS3 : 2KB Upstream Variant
LOC107985414 : 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: 20230706150541

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	115978	C=0.429694	A=0.570306
European	Sub	97764	C=0.42377	A=0.57623
African	Sub	3774	C=0.6025	A=0.3975
African Others	Sub	126	C=0.659	A=0.341
African American	Sub	3648	C=0.6006	A=0.3994
Asian	Sub	3148	C=0.4130	A=0.5870
East Asian	Sub	1928	C=0.4238	A=0.5762
Other Asian	Sub	1220	C=0.3959	A=0.6041
Latin American 1	Sub	174	C=0.414	A=0.586
Latin American 2	Sub	722	C=0.558	A=0.442
South Asian	Sub	120	C=0.275	A=0.725
Other	Sub	10276	C=0.42079	A=0.57921

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=0.500514	A=0.499486
gnomAD - Genomes	Global	Study-wide	140110	C=0.496246	A=0.503754
gnomAD - Genomes	European	Sub	75874	C=0.43936	A=0.56064
gnomAD - Genomes	African	Sub	41986	C=0.60473	A=0.39527
gnomAD - Genomes	American	Sub	13642	C=0.54354	A=0.45646
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	C=0.3489	A=0.6511
gnomAD - Genomes	East Asian	Sub	3132	C=0.3934	A=0.6066
gnomAD - Genomes	Other	Sub	2154	C=0.4629	A=0.5371
Allele Frequency Aggregator	Total	Global	115858	C=0.429707	A=0.570293
Allele Frequency Aggregator	European	Sub	97662	C=0.42380	A=0.57620
Allele Frequency Aggregator	Other	Sub	10272	C=0.42095	A=0.57905
Allele Frequency Aggregator	African	Sub	3760	C=0.6021	A=0.3979
Allele Frequency Aggregator	Asian	Sub	3148	C=0.4130	A=0.5870
Allele Frequency Aggregator	Latin American 2	Sub	722	C=0.558	A=0.442
Allele Frequency Aggregator	Latin American 1	Sub	174	C=0.414	A=0.586
Allele Frequency Aggregator	South Asian	Sub	120	C=0.275	A=0.725
The PAGE Study	Global	Study-wide	78696	C=0.52583	A=0.47417
The PAGE Study	AfricanAmerican	Sub	32514	C=0.60463	A=0.39537
The PAGE Study	Mexican	Sub	10810	C=0.55661	A=0.44339
The PAGE Study	Asian	Sub	8316	C=0.3106	A=0.6894
The PAGE Study	PuertoRican	Sub	7918	C=0.4843	A=0.5157
The PAGE Study	NativeHawaiian	Sub	4534	C=0.4118	A=0.5882
The PAGE Study	Cuban	Sub	4228	C=0.4430	A=0.5570
The PAGE Study	Dominican	Sub	3828	C=0.5285	A=0.4715
The PAGE Study	CentralAmerican	Sub	2450	C=0.6192	A=0.3808
The PAGE Study	SouthAmerican	Sub	1982	C=0.5600	A=0.4400
The PAGE Study	NativeAmerican	Sub	1260	C=0.5095	A=0.4905
The PAGE Study	SouthAsian	Sub	856	C=0.298	A=0.702
14KJPN	JAPANESE	Study-wide	28258	C=0.31333	A=0.68667
8.3KJPN	JAPANESE	Study-wide	16760	C=0.31098	A=0.68902
1000Genomes_30x	Global	Study-wide	6404	C=0.4482	A=0.5518
1000Genomes_30x	African	Sub	1786	C=0.6153	A=0.3847
1000Genomes_30x	Europe	Sub	1266	C=0.4005	A=0.5995
1000Genomes_30x	South Asian	Sub	1202	C=0.2438	A=0.7562
1000Genomes_30x	East Asian	Sub	1170	C=0.3513	A=0.6487
1000Genomes_30x	American	Sub	980	C=0.571	A=0.429
1000Genomes	Global	Study-wide	5008	C=0.4343	A=0.5657
1000Genomes	African	Sub	1322	C=0.6150	A=0.3850
1000Genomes	East Asian	Sub	1008	C=0.3413	A=0.6587
1000Genomes	Europe	Sub	1006	C=0.4026	A=0.5974
1000Genomes	South Asian	Sub	978	C=0.229	A=0.771
1000Genomes	American	Sub	694	C=0.561	A=0.439
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.4281	A=0.5719
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.4598	A=0.5402
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.4563	A=0.5437
KOREAN population from KRGDB	KOREAN	Study-wide	2930	C=0.3655	A=0.6345
Korean Genome Project	KOREAN	Study-wide	1832	C=0.3690	A=0.6310
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.461	A=0.539
CNV burdens in cranial meningiomas	Global	Study-wide	792	C=0.432	A=0.568
CNV burdens in cranial meningiomas	CRM	Sub	792	C=0.432	A=0.568
Northern Sweden	ACPOP	Study-wide	600	C=0.460	A=0.540
SGDP_PRJ	Global	Study-wide	434	C=0.258	A=0.742
Qatari	Global	Study-wide	216	C=0.347	A=0.653
A Vietnamese Genetic Variation Database	Global	Study-wide	212	C=0.368	A=0.632
The Danish reference pan genome	Danish	Study-wide	40	C=0.35	A=0.65
Siberian	Global	Study-wide	36	C=0.25	A=0.75
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	12	C=0.33	A=0.67

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 20	NC_000020.11:g.3174762C>A
GRCh37.p13 chr 20	NC_000020.10:g.3155408C>A

Gene: LZTS3, leucine zipper tumor suppressor family member 3 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
LZTS3 transcript variant 2	NM_001282533.2:c.	N/A	Upstream Transcript Variant
LZTS3 transcript variant 1	NM_001365618.1:c.	N/A	Upstream Transcript Variant
LZTS3 transcript variant 3	NM_001367609.1:c.	N/A	Upstream Transcript Variant
LZTS3 transcript variant 4	NM_001388189.1:c.	N/A	Upstream Transcript Variant
LZTS3 transcript variant 5	NM_001388190.1:c.	N/A	Upstream Transcript Variant
LZTS3 transcript variant 7	NM_001388192.1:c.	N/A	Upstream Transcript Variant
LZTS3 transcript variant 8	NM_001388193.1:c.	N/A	Upstream Transcript Variant
LZTS3 transcript variant 6	NM_001388191.1:c.	N/A	N/A
LZTS3 transcript variant X1	XM_011529408.4:c.	N/A	N/A
LZTS3 transcript variant X2	XM_011529409.4:c.	N/A	N/A

Gene: LOC107985414, uncharacterized LOC107985414 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC107985414 transcript	XR_001754477.2: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	C=	A
GRCh38.p14 chr 20	NC_000020.11:g.3174762=	NC_000020.11:g.3174762C>A
GRCh37.p13 chr 20	NC_000020.10:g.3155408=	NC_000020.10:g.3155408C>A

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#.

101 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	WI_SSAHASNP	ss6644662	Feb 20, 2003 (111)
2	SSAHASNP	ss21791426	Apr 05, 2004 (123)
3	ABI	ss44200618	Mar 15, 2006 (126)
4	HGSV	ss77222407	Dec 06, 2007 (129)
5	BGI	ss103716353	Dec 01, 2009 (131)
6	1000GENOMES	ss111625688	Jan 25, 2009 (130)
7	1000GENOMES	ss115379918	Jan 25, 2009 (130)
8	ENSEMBL	ss144320004	Dec 01, 2009 (131)
9	GMI	ss156093965	Dec 01, 2009 (131)
10	COMPLETE_GENOMICS	ss168904815	Jul 04, 2010 (132)
11	COMPLETE_GENOMICS	ss171833798	Jul 04, 2010 (132)
12	BUSHMAN	ss203812129	Jul 04, 2010 (132)
13	BCM-HGSC-SUB	ss208736310	Jul 04, 2010 (132)
14	1000GENOMES	ss228224555	Jul 14, 2010 (132)
15	1000GENOMES	ss237739909	Jul 15, 2010 (132)
16	1000GENOMES	ss243931309	Jul 15, 2010 (132)
17	BL	ss255439010	May 09, 2011 (134)
18	GMI	ss283278461	May 04, 2012 (137)
19	GMI	ss287412781	Apr 25, 2013 (138)
20	PJP	ss292565664	May 09, 2011 (134)
21	ILLUMINA	ss483324844	May 04, 2012 (137)
22	ILLUMINA	ss484179490	May 04, 2012 (137)
23	EXOME_CHIP	ss491557406	May 04, 2012 (137)
24	ILLUMINA	ss535539544	Sep 08, 2015 (146)
25	TISHKOFF	ss566099438	Apr 25, 2013 (138)
26	SSMP	ss661969195	Apr 25, 2013 (138)
27	ILLUMINA	ss780234814	Sep 08, 2015 (146)
28	ILLUMINA	ss780797493	Sep 08, 2015 (146)
29	ILLUMINA	ss782105540	Sep 08, 2015 (146)
30	ILLUMINA	ss783478773	Sep 08, 2015 (146)
31	ILLUMINA	ss835720122	Sep 08, 2015 (146)
32	EVA-GONL	ss994482103	Aug 21, 2014 (142)
33	JMKIDD_LAB	ss1082028293	Aug 21, 2014 (142)
34	1000GENOMES	ss1363857079	Aug 21, 2014 (142)
35	DDI	ss1428978708	Apr 01, 2015 (144)
36	EVA_GENOME_DK	ss1579412987	Apr 01, 2015 (144)
37	EVA_UK10K_ALSPAC	ss1638299236	Apr 01, 2015 (144)
38	EVA_UK10K_TWINSUK	ss1681293269	Apr 01, 2015 (144)
39	EVA_DECODE	ss1698536427	Apr 01, 2015 (144)
40	ILLUMINA	ss1752382927	Sep 08, 2015 (146)
41	HAMMER_LAB	ss1809396086	Sep 08, 2015 (146)
42	ILLUMINA	ss1917944232	Feb 12, 2016 (147)
43	WEILL_CORNELL_DGM	ss1937991030	Feb 12, 2016 (147)
44	ILLUMINA	ss1946545583	Feb 12, 2016 (147)
45	ILLUMINA	ss1959893351	Feb 12, 2016 (147)
46	GENOMED	ss1969077092	Jul 19, 2016 (147)
47	JJLAB	ss2029772253	Sep 14, 2016 (149)
48	USC_VALOUEV	ss2158326263	Dec 20, 2016 (150)
49	HUMAN_LONGEVITY	ss2240898056	Dec 20, 2016 (150)
50	SYSTEMSBIOZJU	ss2629383773	Nov 08, 2017 (151)
51	ILLUMINA	ss2633769083	Nov 08, 2017 (151)
52	GRF	ss2703997923	Nov 08, 2017 (151)
53	GNOMAD	ss2964854221	Nov 08, 2017 (151)
54	SWEGEN	ss3017782078	Nov 08, 2017 (151)
55	ILLUMINA	ss3022095407	Nov 08, 2017 (151)
56	BIOINF_KMB_FNS_UNIBA	ss3028718071	Nov 08, 2017 (151)
57	CSHL	ss3352392115	Nov 08, 2017 (151)
58	ILLUMINA	ss3628337422	Oct 12, 2018 (152)
59	ILLUMINA	ss3628337423	Oct 12, 2018 (152)
60	ILLUMINA	ss3631727259	Oct 12, 2018 (152)
61	ILLUMINA	ss3634823603	Oct 12, 2018 (152)
62	ILLUMINA	ss3640530901	Oct 12, 2018 (152)
63	ILLUMINA	ss3642169446	Oct 12, 2018 (152)
64	ILLUMINA	ss3644775909	Oct 12, 2018 (152)
65	URBANLAB	ss3650958687	Oct 12, 2018 (152)
66	ILLUMINA	ss3652549513	Oct 12, 2018 (152)
67	EGCUT_WGS	ss3684495650	Jul 13, 2019 (153)
68	EVA_DECODE	ss3706452736	Jul 13, 2019 (153)
69	ILLUMINA	ss3725895104	Jul 13, 2019 (153)
70	ACPOP	ss3743200697	Jul 13, 2019 (153)
71	ILLUMINA	ss3744490594	Jul 13, 2019 (153)
72	ILLUMINA	ss3745123494	Jul 13, 2019 (153)
73	EVA	ss3758356401	Jul 13, 2019 (153)
74	PAGE_CC	ss3772032338	Jul 13, 2019 (153)
75	ILLUMINA	ss3772619796	Jul 13, 2019 (153)
76	PACBIO	ss3788584456	Jul 13, 2019 (153)
77	PACBIO	ss3793486938	Jul 13, 2019 (153)
78	PACBIO	ss3798374068	Jul 13, 2019 (153)
79	KHV_HUMAN_GENOMES	ss3821528021	Jul 13, 2019 (153)
80	EVA	ss3835558437	Apr 27, 2020 (154)
81	EVA	ss3841402822	Apr 27, 2020 (154)
82	EVA	ss3846910218	Apr 27, 2020 (154)
83	SGDP_PRJ	ss3888620488	Apr 27, 2020 (154)
84	KRGDB	ss3938801014	Apr 27, 2020 (154)
85	KOGIC	ss3981725196	Apr 27, 2020 (154)
86	EVA	ss3984745900	Apr 27, 2021 (155)
87	EVA	ss3985863565	Apr 27, 2021 (155)
88	TOPMED	ss5080494366	Apr 27, 2021 (155)
89	TOMMO_GENOMICS	ss5228608508	Apr 27, 2021 (155)
90	1000G_HIGH_COVERAGE	ss5307901882	Oct 13, 2022 (156)
91	EVA	ss5315989608	Oct 13, 2022 (156)
92	HUGCELL_USP	ss5500320136	Oct 13, 2022 (156)
93	1000G_HIGH_COVERAGE	ss5613894638	Oct 13, 2022 (156)
94	SANFORD_IMAGENETICS	ss5662758087	Oct 13, 2022 (156)
95	TOMMO_GENOMICS	ss5787530827	Oct 13, 2022 (156)
96	YY_MCH	ss5817769247	Oct 13, 2022 (156)
97	EVA	ss5845370228	Oct 13, 2022 (156)
98	EVA	ss5847912306	Oct 13, 2022 (156)
99	EVA	ss5853044726	Oct 13, 2022 (156)
100	EVA	ss5922464359	Oct 13, 2022 (156)
101	EVA	ss5957655957	Oct 13, 2022 (156)
102	1000Genomes	NC_000020.10 - 3155408	Oct 12, 2018 (152)
103	1000Genomes_30x	NC_000020.11 - 3174762	Oct 13, 2022 (156)
104	The Avon Longitudinal Study of Parents and Children	NC_000020.10 - 3155408	Oct 12, 2018 (152)
105	Genetic variation in the Estonian population	NC_000020.10 - 3155408	Oct 12, 2018 (152)
106	The Danish reference pan genome	NC_000020.10 - 3155408	Apr 27, 2020 (154)
107	gnomAD - Genomes	NC_000020.11 - 3174762	Apr 27, 2021 (155)
108	Genome of the Netherlands Release 5	NC_000020.10 - 3155408	Apr 27, 2020 (154)
109	KOREAN population from KRGDB	NC_000020.10 - 3155408	Apr 27, 2020 (154)
110	Korean Genome Project	NC_000020.11 - 3174762	Apr 27, 2020 (154)
111	Northern Sweden	NC_000020.10 - 3155408	Jul 13, 2019 (153)
112	The PAGE Study	NC_000020.11 - 3174762	Jul 13, 2019 (153)
113	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000020.10 - 3155408	Apr 27, 2021 (155)
114	CNV burdens in cranial meningiomas	NC_000020.10 - 3155408	Apr 27, 2021 (155)
115	Qatari	NC_000020.10 - 3155408	Apr 27, 2020 (154)
116	SGDP_PRJ	NC_000020.10 - 3155408	Apr 27, 2020 (154)
117	Siberian	NC_000020.10 - 3155408	Apr 27, 2020 (154)
118	8.3KJPN	NC_000020.10 - 3155408	Apr 27, 2021 (155)
119	14KJPN	NC_000020.11 - 3174762	Oct 13, 2022 (156)
120	TopMed	NC_000020.11 - 3174762	Apr 27, 2021 (155)
121	UK 10K study - Twins	NC_000020.10 - 3155408	Oct 12, 2018 (152)
122	A Vietnamese Genetic Variation Database	NC_000020.10 - 3155408	Jul 13, 2019 (153)
123	ALFA	NC_000020.11 - 3174762	Apr 27, 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)
rs13043384	Sep 24, 2004 (123)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss77222407, ss111625688, ss115379918, ss168904815, ss171833798, ss203812129, ss208736310, ss255439010, ss283278461, ss287412781, ss292565664, ss484179490, ss1698536427	NC_000020.9:3103407:C:A	NC_000020.11:3174761:C:A	(self)
77289106, 42780641, 30233898, 5577926, 19061847, 45978408, 16485562, 1089492, 295466, 20032952, 40637468, 10842617, 86577815, 42780641, 9444032, ss228224555, ss237739909, ss243931309, ss483324844, ss491557406, ss535539544, ss566099438, ss661969195, ss780234814, ss780797493, ss782105540, ss783478773, ss835720122, ss994482103, ss1082028293, ss1363857079, ss1428978708, ss1579412987, ss1638299236, ss1681293269, ss1752382927, ss1809396086, ss1917944232, ss1937991030, ss1946545583, ss1959893351, ss1969077092, ss2029772253, ss2158326263, ss2629383773, ss2633769083, ss2703997923, ss2964854221, ss3017782078, ss3022095407, ss3352392115, ss3628337422, ss3628337423, ss3631727259, ss3634823603, ss3640530901, ss3642169446, ss3644775909, ss3652549513, ss3684495650, ss3743200697, ss3744490594, ss3745123494, ss3758356401, ss3772619796, ss3788584456, ss3793486938, ss3798374068, ss3835558437, ss3841402822, ss3888620488, ss3938801014, ss3984745900, ss3985863565, ss5228608508, ss5315989608, ss5662758087, ss5845370228, ss5847912306, ss5957655957	NC_000020.10:3155407:C:A	NC_000020.11:3174761:C:A	(self)
101420573, 545014883, 38103197, 1253807, 121367931, 355603311, 14214845474, ss2240898056, ss3028718071, ss3650958687, ss3706452736, ss3725895104, ss3772032338, ss3821528021, ss3846910218, ss3981725196, ss5080494366, ss5307901882, ss5500320136, ss5613894638, ss5787530827, ss5817769247, ss5853044726, ss5922464359	NC_000020.11:3174761:C:A	NC_000020.11:3174761:C:A	(self)
ss6644662, ss21791426, ss44200618, ss103716353, ss144320004, ss156093965	NT_011387.8:3095407:C:A	NC_000020.11:3174761:C:A	(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 rs4813630

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

rs4813630