Name: rs1836
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.

rs1836

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:3829552 (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>G
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.099758 (26405/264690, TOPMED)
A=0.084218 (11810/140232, GnomAD)
A=0.40038 (11314/28258, 14KJPN) (+ 18 more)
A=0.07275 (1382/18996, ALFA)
A=0.39875 (6683/16760, 8.3KJPN)
A=0.2030 (1300/6404, 1000G_30x)
A=0.2105 (1054/5008, 1000G)
A=0.0681 (305/4480, Estonian)
A=0.0529 (204/3854, ALSPAC)
A=0.0445 (165/3708, TWINSUK)
G=0.4976 (1457/2928, KOREAN)
G=0.4787 (877/1832, Korea1K)
A=0.1101 (124/1126, Daghestan)
A=0.045 (45/998, GoNL)
A=0.063 (38/600, NorthernSweden)
A=0.145 (72/498, SGDP_PRJ)
A=0.111 (24/216, Qatari)
G=0.407 (87/214, Vietnamese)
A=0.00 (0/56, Ancient Sardinia)
A=0.27 (14/52, Siberian)
A=0.12 (5/40, GENOME_DK)

Clinical Significance: Reported in ClinVar
Gene : Consequence: CEP104 : 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	18996	A=0.07275	G=0.92725
European	Sub	14370	A=0.05651	G=0.94349
African	Sub	2950	A=0.0902	G=0.9098
African Others	Sub	114	A=0.070	G=0.930
African American	Sub	2836	A=0.0910	G=0.9090
Asian	Sub	114	A=0.439	G=0.561
East Asian	Sub	88	A=0.45	G=0.55
Other Asian	Sub	26	A=0.38	G=0.62
Latin American 1	Sub	146	A=0.103	G=0.897
Latin American 2	Sub	610	A=0.208	G=0.792
South Asian	Sub	100	A=0.34	G=0.66
Other	Sub	706	A=0.110	G=0.890

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	A=0.099758	G=0.900242
gnomAD - Genomes	Global	Study-wide	140232	A=0.084218	G=0.915782
gnomAD - Genomes	European	Sub	75946	A=0.05604	G=0.94396
gnomAD - Genomes	African	Sub	42030	A=0.09122	G=0.90878
gnomAD - Genomes	American	Sub	13656	A=0.12705	G=0.87295
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	A=0.0367	G=0.9633
gnomAD - Genomes	East Asian	Sub	3124	A=0.5294	G=0.4706
gnomAD - Genomes	Other	Sub	2152	A=0.0971	G=0.9029
14KJPN	JAPANESE	Study-wide	28258	A=0.40038	G=0.59962
Allele Frequency Aggregator	Total	Global	18996	A=0.07275	G=0.92725
Allele Frequency Aggregator	European	Sub	14370	A=0.05651	G=0.94349
Allele Frequency Aggregator	African	Sub	2950	A=0.0902	G=0.9098
Allele Frequency Aggregator	Other	Sub	706	A=0.110	G=0.890
Allele Frequency Aggregator	Latin American 2	Sub	610	A=0.208	G=0.792
Allele Frequency Aggregator	Latin American 1	Sub	146	A=0.103	G=0.897
Allele Frequency Aggregator	Asian	Sub	114	A=0.439	G=0.561
Allele Frequency Aggregator	South Asian	Sub	100	A=0.34	G=0.66
8.3KJPN	JAPANESE	Study-wide	16760	A=0.39875	G=0.60125
1000Genomes_30x	Global	Study-wide	6404	A=0.2030	G=0.7970
1000Genomes_30x	African	Sub	1786	A=0.0862	G=0.9138
1000Genomes_30x	Europe	Sub	1266	A=0.0592	G=0.9408
1000Genomes_30x	South Asian	Sub	1202	A=0.2829	G=0.7171
1000Genomes_30x	East Asian	Sub	1170	A=0.5162	G=0.4838
1000Genomes_30x	American	Sub	980	A=0.130	G=0.870
1000Genomes	Global	Study-wide	5008	A=0.2105	G=0.7895
1000Genomes	African	Sub	1322	A=0.0802	G=0.9198
1000Genomes	East Asian	Sub	1008	A=0.5208	G=0.4792
1000Genomes	Europe	Sub	1006	A=0.0557	G=0.9443
1000Genomes	South Asian	Sub	978	A=0.282	G=0.718
1000Genomes	American	Sub	694	A=0.131	G=0.869
Genetic variation in the Estonian population	Estonian	Study-wide	4480	A=0.0681	G=0.9319
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.0529	G=0.9471
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.0445	G=0.9555
KOREAN population from KRGDB	KOREAN	Study-wide	2928	A=0.5024	G=0.4976
Korean Genome Project	KOREAN	Study-wide	1832	A=0.5213	G=0.4787
Genome-wide autozygosity in Daghestan	Global	Study-wide	1126	A=0.1101	G=0.8899
Genome-wide autozygosity in Daghestan	Daghestan	Sub	626	A=0.065	G=0.935
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	A=0.146	G=0.854
Genome-wide autozygosity in Daghestan	Central Asia	Sub	118	A=0.254	G=0.746
Genome-wide autozygosity in Daghestan	Europe	Sub	106	A=0.047	G=0.953
Genome-wide autozygosity in Daghestan	South Asian	Sub	96	A=0.28	G=0.72
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	A=0.00	G=1.00
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	A=0.045	G=0.955
Northern Sweden	ACPOP	Study-wide	600	A=0.063	G=0.937
SGDP_PRJ	Global	Study-wide	498	A=0.145	G=0.855
Qatari	Global	Study-wide	216	A=0.111	G=0.889
A Vietnamese Genetic Variation Database	Global	Study-wide	214	A=0.593	G=0.407
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	56	A=0.00	G=1.00
Siberian	Global	Study-wide	52	A=0.27	G=0.73
The Danish reference pan genome	Danish	Study-wide	40	A=0.12	G=0.88

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.3829552A>G
GRCh37.p13 chr 1	NC_000001.10:g.3746116A>G
CEP104 RefSeqGene	NG_046726.1:g.32682T>C
LOC126805586 genomic region	NG_081911.1:g.335A>G

Gene: CEP104, centrosomal protein 104 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CEP104 transcript	NM_014704.4:c.2044-179T>C	N/A	Intron Variant
CEP104 transcript variant X2	XM_005244815.5:c.2152-179… XM_005244815.5:c.2152-179T>C	N/A	Intron Variant
CEP104 transcript variant X1	XM_024451101.2:c.2170-179… XM_024451101.2:c.2170-179T>C	N/A	Intron Variant
CEP104 transcript variant X3	XM_024451102.2:c.1996-179… XM_024451102.2:c.1996-179T>C	N/A	Intron Variant
CEP104 transcript variant X5	XM_024451104.2:c.1972-179… XM_024451104.2:c.1972-179T>C	N/A	Intron Variant
CEP104 transcript variant X7	XM_024451106.2:c.1798-179… XM_024451106.2:c.1798-179T>C	N/A	Intron Variant
CEP104 transcript variant X8	XM_024451108.2:c.2170-179… XM_024451108.2:c.2170-179T>C	N/A	Intron Variant
CEP104 transcript variant X4	XM_047435158.1:c.1978-179… XM_047435158.1:c.1978-179T>C	N/A	Intron Variant
CEP104 transcript variant X6	XM_047435161.1:c.1954-179… XM_047435161.1:c.1954-179T>C	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.

Allele: G (allele ID: 1231598 )

ClinVar Accession	Disease Names	Clinical Significance
RCV001643260.2	not provided	Benign

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=	G
GRCh38.p14 chr 1	NC_000001.11:g.3829552=	NC_000001.11:g.3829552A>G
GRCh37.p13 chr 1	NC_000001.10:g.3746116=	NC_000001.10:g.3746116A>G
CEP104 RefSeqGene	NG_046726.1:g.32682=	NG_046726.1:g.32682T>C
LOC126805586 genomic region	NG_081911.1:g.335=	NG_081911.1:g.335A>G
CEP104 transcript	NM_014704.3:c.2044-179=	NM_014704.3:c.2044-179T>C
CEP104 transcript	NM_014704.4:c.2044-179=	NM_014704.4:c.2044-179T>C
CEP104 transcript variant X1	XM_005244815.1:c.2152-179=	XM_005244815.1:c.2152-179T>C
CEP104 transcript variant X2	XM_005244815.5:c.2152-179=	XM_005244815.5:c.2152-179T>C
CEP104 transcript variant X1	XM_024451101.2:c.2170-179=	XM_024451101.2:c.2170-179T>C
CEP104 transcript variant X3	XM_024451102.2:c.1996-179=	XM_024451102.2:c.1996-179T>C
CEP104 transcript variant X5	XM_024451104.2:c.1972-179=	XM_024451104.2:c.1972-179T>C
CEP104 transcript variant X7	XM_024451106.2:c.1798-179=	XM_024451106.2:c.1798-179T>C
CEP104 transcript variant X8	XM_024451108.2:c.2170-179=	XM_024451108.2:c.2170-179T>C
CEP104 transcript variant X4	XM_047435158.1:c.1978-179=	XM_047435158.1:c.1978-179T>C
CEP104 transcript variant X6	XM_047435161.1:c.1954-179=	XM_047435161.1:c.1954-179T>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#.

87 SubSNP, 21 Frequency, 1 ClinVar submissions

No	Submitter	Submission ID	Date (Build)
1	WIAF	ss1861	Sep 19, 2000 (36)
2	YUSUKE	ss5005425	Aug 28, 2002 (108)
3	SC_SNP	ss12992584	Dec 05, 2003 (119)
4	CSHL-HAPMAP	ss16427208	Feb 27, 2004 (120)
5	CSHL-HAPMAP	ss17353932	Feb 27, 2004 (120)
6	SSAHASNP	ss20463184	Apr 05, 2004 (121)
7	PERLEGEN	ss23842215	Sep 20, 2004 (123)
8	ABI	ss44131842	Mar 14, 2006 (126)
9	HGSV	ss81115463	Dec 14, 2007 (130)
10	HGSV	ss81617175	Dec 14, 2007 (130)
11	HGSV	ss84156712	Dec 14, 2007 (130)
12	BCMHGSC_JDW	ss87174544	Mar 23, 2008 (129)
13	HUMANGENOME_JCVI	ss97915520	Feb 03, 2009 (130)
14	1000GENOMES	ss107949149	Jan 22, 2009 (130)
15	1000GENOMES	ss109967826	Jan 24, 2009 (130)
16	ILLUMINA-UK	ss118453633	Feb 14, 2009 (130)
17	ENSEMBL	ss137763658	Dec 01, 2009 (131)
18	ENSEMBL	ss138971175	Dec 01, 2009 (131)
19	GMI	ss154559515	Dec 01, 2009 (131)
20	COMPLETE_GENOMICS	ss163005135	Jul 04, 2010 (132)
21	COMPLETE_GENOMICS	ss163738616	Jul 04, 2010 (132)
22	BUSHMAN	ss197925350	Jul 04, 2010 (132)
23	BCM-HGSC-SUB	ss205280462	Jul 04, 2010 (132)
24	1000GENOMES	ss218203369	Jul 14, 2010 (132)
25	1000GENOMES	ss230404238	Jul 14, 2010 (132)
26	1000GENOMES	ss238123112	Jul 15, 2010 (132)
27	BL	ss252880611	May 09, 2011 (134)
28	GMI	ss275691523	May 04, 2012 (137)
29	GMI	ss283991046	Apr 25, 2013 (138)
30	PJP	ss290498365	May 09, 2011 (134)
31	TISHKOFF	ss553734798	Apr 25, 2013 (138)
32	SSMP	ss647536606	Apr 25, 2013 (138)
33	EVA-GONL	ss974796656	Aug 21, 2014 (142)
34	JMKIDD_LAB	ss1067627438	Aug 21, 2014 (142)
35	1000GENOMES	ss1289452280	Aug 21, 2014 (142)
36	HAMMER_LAB	ss1397238574	Sep 08, 2015 (146)
37	DDI	ss1425693093	Apr 01, 2015 (144)
38	EVA_GENOME_DK	ss1573860226	Apr 01, 2015 (144)
39	EVA_DECODE	ss1584155406	Apr 01, 2015 (144)
40	EVA_UK10K_ALSPAC	ss1599427701	Apr 01, 2015 (144)
41	EVA_UK10K_TWINSUK	ss1642421734	Apr 01, 2015 (144)
42	HAMMER_LAB	ss1793785259	Sep 08, 2015 (146)
43	WEILL_CORNELL_DGM	ss1917992176	Feb 12, 2016 (147)
44	GENOMED	ss1966671431	Jul 19, 2016 (147)
45	JJLAB	ss2019512265	Sep 14, 2016 (149)
46	USC_VALOUEV	ss2147502624	Dec 20, 2016 (150)
47	HUMAN_LONGEVITY	ss2159575812	Dec 20, 2016 (150)
48	SYSTEMSBIOZJU	ss2624271902	Nov 08, 2017 (151)
49	GRF	ss2697396677	Nov 08, 2017 (151)
50	GNOMAD	ss2750973858	Nov 08, 2017 (151)
51	SWEGEN	ss2986201578	Nov 08, 2017 (151)
52	BIOINF_KMB_FNS_UNIBA	ss3023519756	Nov 08, 2017 (151)
53	CSHL	ss3343289057	Nov 08, 2017 (151)
54	OMUKHERJEE_ADBS	ss3646220221	Oct 11, 2018 (152)
55	URBANLAB	ss3646586813	Oct 11, 2018 (152)
56	EGCUT_WGS	ss3654302793	Jul 12, 2019 (153)
57	EVA_DECODE	ss3686047515	Jul 12, 2019 (153)
58	ACPOP	ss3726740209	Jul 12, 2019 (153)
59	EVA	ss3745755571	Jul 12, 2019 (153)
60	PACBIO	ss3783308845	Jul 12, 2019 (153)
61	PACBIO	ss3788985731	Jul 12, 2019 (153)
62	PACBIO	ss3793858358	Jul 12, 2019 (153)
63	KHV_HUMAN_GENOMES	ss3798777230	Jul 12, 2019 (153)
64	EVA	ss3825994066	Apr 25, 2020 (154)
65	EVA	ss3836384219	Apr 25, 2020 (154)
66	EVA	ss3841788387	Apr 25, 2020 (154)
67	SGDP_PRJ	ss3848069843	Apr 25, 2020 (154)
68	KRGDB	ss3892931494	Apr 25, 2020 (154)
69	KOGIC	ss3943693185	Apr 25, 2020 (154)
70	EVA	ss3984774957	Apr 25, 2021 (155)
71	TOPMED	ss4437309896	Apr 25, 2021 (155)
72	TOMMO_GENOMICS	ss5142202327	Apr 25, 2021 (155)
73	1000G_HIGH_COVERAGE	ss5240968726	Oct 13, 2022 (156)
74	EVA	ss5316374668	Oct 13, 2022 (156)
75	HUGCELL_USP	ss5442194336	Oct 13, 2022 (156)
76	EVA	ss5505751696	Oct 13, 2022 (156)
77	1000G_HIGH_COVERAGE	ss5512634709	Oct 13, 2022 (156)
78	SANFORD_IMAGENETICS	ss5624808947	Oct 13, 2022 (156)
79	TOMMO_GENOMICS	ss5666416240	Oct 13, 2022 (156)
80	EVA	ss5800077082	Oct 13, 2022 (156)
81	YY_MCH	ss5800271804	Oct 13, 2022 (156)
82	EVA	ss5831459924	Oct 13, 2022 (156)
83	EVA	ss5848759263	Oct 13, 2022 (156)
84	EVA	ss5906811539	Oct 13, 2022 (156)
85	EVA	ss5936633661	Oct 13, 2022 (156)
86	EVA	ss5979928745	Oct 13, 2022 (156)
87	EVA	ss5981189786	Oct 13, 2022 (156)
88	1000Genomes	NC_000001.10 - 3746116	Oct 11, 2018 (152)
89	1000Genomes_30x	NC_000001.11 - 3829552	Oct 13, 2022 (156)
90	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 3746116	Oct 11, 2018 (152)
91	Genome-wide autozygosity in Daghestan	NC_000001.9 - 3735976	Apr 25, 2020 (154)
92	Genetic variation in the Estonian population	NC_000001.10 - 3746116	Oct 11, 2018 (152)
93	The Danish reference pan genome	NC_000001.10 - 3746116	Apr 25, 2020 (154)
94	gnomAD - Genomes	NC_000001.11 - 3829552	Apr 25, 2021 (155)
95	Genome of the Netherlands Release 5	NC_000001.10 - 3746116	Apr 25, 2020 (154)
96	KOREAN population from KRGDB	NC_000001.10 - 3746116	Apr 25, 2020 (154)
97	Korean Genome Project	NC_000001.11 - 3829552	Apr 25, 2020 (154)
98	Northern Sweden	NC_000001.10 - 3746116	Jul 12, 2019 (153)
99	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000001.10 - 3746116	Apr 25, 2021 (155)
100	Qatari	NC_000001.10 - 3746116	Apr 25, 2020 (154)
101	SGDP_PRJ	NC_000001.10 - 3746116	Apr 25, 2020 (154)
102	Siberian	NC_000001.10 - 3746116	Apr 25, 2020 (154)
103	8.3KJPN	NC_000001.10 - 3746116	Apr 25, 2021 (155)
104	14KJPN	NC_000001.11 - 3829552	Oct 13, 2022 (156)
105	TopMed	NC_000001.11 - 3829552	Apr 25, 2021 (155)
106	UK 10K study - Twins	NC_000001.10 - 3746116	Oct 11, 2018 (152)
107	A Vietnamese Genetic Variation Database	NC_000001.10 - 3746116	Jul 12, 2019 (153)
108	ALFA	NC_000001.11 - 3829552	Apr 25, 2021 (155)
109	ClinVar	RCV001643260.2	Oct 13, 2022 (156)

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)
rs3819010	Oct 08, 2002 (108)
rs56926330	May 23, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss81115463, ss81617175, ss84156712	NC_000001.8:3769272:A:G	NC_000001.11:3829551:A:G	(self)
61, ss87174544, ss107949149, ss109967826, ss118453633, ss163005135, ss163738616, ss197925350, ss205280462, ss252880611, ss275691523, ss283991046, ss290498365, ss1397238574, ss1584155406	NC_000001.9:3735975:A:G	NC_000001.11:3829551:A:G	(self)
120321, 53964, 41041, 1367460, 23259, 108888, 25074, 884, 34106, 86823, 18978, 171634, 53964, 11436, ss218203369, ss230404238, ss238123112, ss553734798, ss647536606, ss974796656, ss1067627438, ss1289452280, ss1425693093, ss1573860226, ss1599427701, ss1642421734, ss1793785259, ss1917992176, ss1966671431, ss2019512265, ss2147502624, ss2624271902, ss2697396677, ss2750973858, ss2986201578, ss3343289057, ss3646220221, ss3654302793, ss3726740209, ss3745755571, ss3783308845, ss3788985731, ss3793858358, ss3825994066, ss3836384219, ss3848069843, ss3892931494, ss3984774957, ss5142202327, ss5316374668, ss5505751696, ss5624808947, ss5800077082, ss5831459924, ss5936633661, ss5979928745, ss5981189786	NC_000001.10:3746115:A:G	NC_000001.11:3829551:A:G	(self)
RCV001643260.2, 160644, 867188, 71186, 253344, 916231, 10947058125, ss2159575812, ss3023519756, ss3646586813, ss3686047515, ss3798777230, ss3841788387, ss3943693185, ss4437309896, ss5240968726, ss5442194336, ss5512634709, ss5666416240, ss5800271804, ss5848759263, ss5906811539	NC_000001.11:3829551:A:G	NC_000001.11:3829551:A:G	(self)
ss12992584, ss16427208, ss17353932, ss20463184	NT_004321.15:1052889:A:G	NC_000001.11:3829551:A:G	(self)
ss1861, ss5005425, ss23842215, ss44131842, ss97915520, ss137763658, ss138971175, ss154559515	NT_004350.19:3224747:A:G	NC_000001.11:3829551:A:G	(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 rs1836

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

rs1836