Name: rs4861
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.

rs4861

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr17:78992110 (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>T
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.158869 (42051/264690, TOPMED)
T=0.120878 (22267/184210, ALFA)
T=0.142459 (19971/140188, GnomAD) (+ 21 more)
T=0.20934 (16475/78700, PAGE_STUDY)
T=0.24595 (6950/28258, 14KJPN)
T=0.24230 (4061/16760, 8.3KJPN)
T=0.2163 (1385/6404, 1000G_30x)
T=0.2117 (1060/5008, 1000G)
T=0.1330 (596/4480, Estonian)
T=0.1214 (468/3854, ALSPAC)
T=0.1154 (428/3708, TWINSUK)
T=0.2628 (770/2930, KOREAN)
T=0.1686 (317/1880, HapMap)
T=0.2822 (517/1832, Korea1K)
T=0.130 (130/998, GoNL)
T=0.268 (212/792, PRJEB37584)
T=0.125 (75/600, NorthernSweden)
T=0.074 (16/216, Qatari)
T=0.354 (75/212, Vietnamese)
C=0.371 (72/194, SGDP_PRJ)
T=0.10 (10/100, Ancient Sardinia)
T=0.05 (2/40, GENOME_DK)
C=0.50 (6/12, Siberian)
T=0.50 (6/12, Siberian)

Clinical Significance: Reported in ClinVar
Gene : Consequence: CANT1 : 3 Prime UTR 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	189246	C=0.878692	T=0.121308
European	Sub	163976	C=0.888789	T=0.111211
African	Sub	10690	C=0.85323	T=0.14677
African Others	Sub	414	C=0.816	T=0.184
African American	Sub	10276	C=0.85471	T=0.14529
Asian	Sub	3544	C=0.7201	T=0.2799
East Asian	Sub	2848	C=0.7293	T=0.2707
Other Asian	Sub	696	C=0.682	T=0.318
Latin American 1	Sub	926	C=0.841	T=0.159
Latin American 2	Sub	2314	C=0.6763	T=0.3237
South Asian	Sub	332	C=0.720	T=0.280
Other	Sub	7464	C=0.8431	T=0.1569

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=0.841131	T=0.158869
Allele Frequency Aggregator	Total	Global	184210	C=0.879122	T=0.120878
Allele Frequency Aggregator	European	Sub	160882	C=0.888844	T=0.111156
Allele Frequency Aggregator	African	Sub	9548	C=0.8537	T=0.1463
Allele Frequency Aggregator	Other	Sub	6664	C=0.8490	T=0.1510
Allele Frequency Aggregator	Asian	Sub	3544	C=0.7201	T=0.2799
Allele Frequency Aggregator	Latin American 2	Sub	2314	C=0.6763	T=0.3237
Allele Frequency Aggregator	Latin American 1	Sub	926	C=0.841	T=0.159
Allele Frequency Aggregator	South Asian	Sub	332	C=0.720	T=0.280
gnomAD - Genomes	Global	Study-wide	140188	C=0.857541	T=0.142459
gnomAD - Genomes	European	Sub	75920	C=0.88633	T=0.11367
gnomAD - Genomes	African	Sub	42014	C=0.85550	T=0.14450
gnomAD - Genomes	American	Sub	13656	C=0.73521	T=0.26479
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	C=0.9088	T=0.0912
gnomAD - Genomes	East Asian	Sub	3122	C=0.6768	T=0.3232
gnomAD - Genomes	Other	Sub	2152	C=0.8411	T=0.1589
The PAGE Study	Global	Study-wide	78700	C=0.79066	T=0.20934
The PAGE Study	AfricanAmerican	Sub	32514	C=0.85332	T=0.14668
The PAGE Study	Mexican	Sub	10810	C=0.65837	T=0.34163
The PAGE Study	Asian	Sub	8318	C=0.7418	T=0.2582
The PAGE Study	PuertoRican	Sub	7918	C=0.8155	T=0.1845
The PAGE Study	NativeHawaiian	Sub	4534	C=0.7097	T=0.2903
The PAGE Study	Cuban	Sub	4230	C=0.8610	T=0.1390
The PAGE Study	Dominican	Sub	3828	C=0.8568	T=0.1432
The PAGE Study	CentralAmerican	Sub	2450	C=0.6649	T=0.3351
The PAGE Study	SouthAmerican	Sub	1982	C=0.6811	T=0.3189
The PAGE Study	NativeAmerican	Sub	1260	C=0.7762	T=0.2238
The PAGE Study	SouthAsian	Sub	856	C=0.746	T=0.254
14KJPN	JAPANESE	Study-wide	28258	C=0.75405	T=0.24595
8.3KJPN	JAPANESE	Study-wide	16760	C=0.75770	T=0.24230
1000Genomes_30x	Global	Study-wide	6404	C=0.7837	T=0.2163
1000Genomes_30x	African	Sub	1786	C=0.8578	T=0.1422
1000Genomes_30x	Europe	Sub	1266	C=0.8926	T=0.1074
1000Genomes_30x	South Asian	Sub	1202	C=0.7396	T=0.2604
1000Genomes_30x	East Asian	Sub	1170	C=0.6692	T=0.3308
1000Genomes_30x	American	Sub	980	C=0.699	T=0.301
1000Genomes	Global	Study-wide	5008	C=0.7883	T=0.2117
1000Genomes	African	Sub	1322	C=0.8646	T=0.1354
1000Genomes	East Asian	Sub	1008	C=0.6796	T=0.3204
1000Genomes	Europe	Sub	1006	C=0.8936	T=0.1064
1000Genomes	South Asian	Sub	978	C=0.758	T=0.242
1000Genomes	American	Sub	694	C=0.692	T=0.308
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.8670	T=0.1330
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.8786	T=0.1214
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.8846	T=0.1154
KOREAN population from KRGDB	KOREAN	Study-wide	2930	C=0.7372	T=0.2628
HapMap	Global	Study-wide	1880	C=0.8314	T=0.1686
HapMap	American	Sub	764	C=0.784	T=0.216
HapMap	African	Sub	686	C=0.885	T=0.115
HapMap	Asian	Sub	254	C=0.772	T=0.228
HapMap	Europe	Sub	176	C=0.915	T=0.085
Korean Genome Project	KOREAN	Study-wide	1832	C=0.7178	T=0.2822
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.870	T=0.130
CNV burdens in cranial meningiomas	Global	Study-wide	792	C=0.732	T=0.268
CNV burdens in cranial meningiomas	CRM	Sub	792	C=0.732	T=0.268
Northern Sweden	ACPOP	Study-wide	600	C=0.875	T=0.125
Qatari	Global	Study-wide	216	C=0.926	T=0.074
A Vietnamese Genetic Variation Database	Global	Study-wide	212	C=0.646	T=0.354
SGDP_PRJ	Global	Study-wide	194	C=0.371	T=0.629
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	100	C=0.90	T=0.10
The Danish reference pan genome	Danish	Study-wide	40	C=0.95	T=0.05
Siberian	Global	Study-wide	12	C=0.50	T=0.50

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 17	NC_000017.11:g.78992110C>T
GRCh37.p13 chr 17	NC_000017.10:g.76988192C>T
CANT1 RefSeqGene	NG_016645.1:g.22708G>A

Gene: CANT1, calcium activated nucleotidase 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CANT1 transcript variant 3	NM_001159773.2:c.*1440=	N/A	3 Prime UTR Variant
CANT1 transcript variant 1	NM_138793.4:c.*1440=	N/A	3 Prime UTR Variant
CANT1 transcript variant 2	NM_001159772.2:c.*1440=	N/A	3 Prime UTR 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: T (allele ID: 347588 )

ClinVar Accession	Disease Names	Clinical Significance
RCV000389226.3	Desbuquois dysplasia 1	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	C=	T
GRCh38.p14 chr 17	NC_000017.11:g.78992110=	NC_000017.11:g.78992110C>T
GRCh37.p13 chr 17	NC_000017.10:g.76988192=	NC_000017.10:g.76988192C>T
CANT1 RefSeqGene	NG_016645.1:g.22708=	NG_016645.1:g.22708G>A
CANT1 transcript variant 1	NM_138793.4:c.*1440=	NM_138793.4:c.*1440G>A
CANT1 transcript variant 1	NM_138793.3:c.*1440=	NM_138793.3:c.*1440G>A
CANT1 transcript variant 2	NM_001159772.2:c.*1440=	NM_001159772.2:c.*1440G>A
CANT1 transcript variant 2	NM_001159772.1:c.*1440=	NM_001159772.1:c.*1440G>A
CANT1 transcript variant 3	NM_001159773.2:c.*1440=	NM_001159773.2:c.*1440G>A
CANT1 transcript variant 3	NM_001159773.1:c.*1440=	NM_001159773.1:c.*1440G>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#.

113 SubSNP, 23 Frequency, 1 ClinVar submissions

No	Submitter	Submission ID	Date (Build)
1	CGAP-GAI	ss13020	Sep 19, 2000 (52)
2	CGAP-GAI	ss18193	Sep 19, 2000 (52)
3	TSC-CSHL	ss3336757	Sep 28, 2001 (126)
4	LEE	ss4441764	May 29, 2002 (106)
5	SC_JCM	ss6184861	Feb 20, 2003 (111)
6	WI_SSAHASNP	ss6609880	Feb 20, 2003 (111)
7	CGAP-GAI	ss16243667	Feb 27, 2004 (120)
8	CSHL-HAPMAP	ss19373831	Feb 27, 2004 (120)
9	PERLEGEN	ss24118740	Sep 20, 2004 (123)
10	SEQUENOM	ss24793372	Sep 20, 2004 (123)
11	ABI	ss44033020	Mar 10, 2006 (126)
12	ILLUMINA	ss65743149	Oct 14, 2006 (127)
13	ILLUMINA	ss74869323	Dec 07, 2007 (129)
14	HGSV	ss83670583	Dec 15, 2007 (130)
15	1000GENOMES	ss113883218	Jan 25, 2009 (130)
16	ILLUMINA-UK	ss118138913	Feb 14, 2009 (130)
17	KRIBB_YJKIM	ss119337473	Dec 01, 2009 (131)
18	GMI	ss154683238	Dec 01, 2009 (131)
19	ILLUMINA	ss160720801	Dec 01, 2009 (131)
20	ENSEMBL	ss161841322	Dec 01, 2009 (131)
21	COMPLETE_GENOMICS	ss170321734	Jul 04, 2010 (132)
22	COMPLETE_GENOMICS	ss171768974	Jul 04, 2010 (132)
23	ILLUMINA	ss173848511	Jul 04, 2010 (132)
24	BUSHMAN	ss202825057	Jul 04, 2010 (132)
25	1000GENOMES	ss227674236	Jul 14, 2010 (132)
26	1000GENOMES	ss237334107	Jul 15, 2010 (132)
27	1000GENOMES	ss243611286	Jul 15, 2010 (132)
28	BL	ss255808782	May 09, 2011 (134)
29	GMI	ss282854814	May 04, 2012 (137)
30	GMI	ss287221141	Apr 25, 2013 (138)
31	ILLUMINA	ss481077161	May 04, 2012 (137)
32	ILLUMINA	ss481099078	May 04, 2012 (137)
33	ILLUMINA	ss482092240	Sep 08, 2015 (146)
34	ILLUMINA	ss485333708	May 04, 2012 (137)
35	ILLUMINA	ss537285244	Sep 08, 2015 (146)
36	TISHKOFF	ss565427623	Apr 25, 2013 (138)
37	SSMP	ss661242773	Apr 25, 2013 (138)
38	ILLUMINA	ss778550358	Sep 08, 2015 (146)
39	ILLUMINA	ss783112626	Sep 08, 2015 (146)
40	ILLUMINA	ss784069583	Sep 08, 2015 (146)
41	ILLUMINA	ss832371309	Sep 08, 2015 (146)
42	ILLUMINA	ss834007083	Sep 08, 2015 (146)
43	EVA-GONL	ss993367143	Aug 21, 2014 (142)
44	JMKIDD_LAB	ss1081239604	Aug 21, 2014 (142)
45	1000GENOMES	ss1359670076	Aug 21, 2014 (142)
46	EVA_GENOME_DK	ss1578258125	Apr 01, 2015 (144)
47	EVA_UK10K_ALSPAC	ss1636171690	Apr 01, 2015 (144)
48	EVA_UK10K_TWINSUK	ss1679165723	Apr 01, 2015 (144)
49	EVA_DECODE	ss1697419312	Apr 01, 2015 (144)
50	EVA_SVP	ss1713600696	Apr 01, 2015 (144)
51	ILLUMINA	ss1752242571	Sep 08, 2015 (146)
52	WEILL_CORNELL_DGM	ss1936832347	Feb 12, 2016 (147)
53	ILLUMINA	ss1946476273	Feb 12, 2016 (147)
54	ILLUMINA	ss1959774367	Feb 12, 2016 (147)
55	GENOMED	ss1968441946	Jul 19, 2016 (147)
56	JJLAB	ss2029187877	Sep 14, 2016 (149)
57	USC_VALOUEV	ss2157676355	Dec 20, 2016 (150)
58	HUMAN_LONGEVITY	ss2218885777	Dec 20, 2016 (150)
59	SYSTEMSBIOZJU	ss2629089707	Nov 08, 2017 (151)
60	ILLUMINA	ss2633429503	Nov 08, 2017 (151)
61	GRF	ss2702243103	Nov 08, 2017 (151)
62	ILLUMINA	ss2710858384	Nov 08, 2017 (151)
63	GNOMAD	ss2952822371	Nov 08, 2017 (151)
64	SWEGEN	ss3015958099	Nov 08, 2017 (151)
65	ILLUMINA	ss3021809513	Nov 08, 2017 (151)
66	BIOINF_KMB_FNS_UNIBA	ss3028417071	Nov 08, 2017 (151)
67	CSHL	ss3351855711	Nov 08, 2017 (151)
68	ILLUMINA	ss3625719064	Oct 12, 2018 (152)
69	ILLUMINA	ss3627731298	Oct 12, 2018 (152)
70	ILLUMINA	ss3631408580	Oct 12, 2018 (152)
71	ILLUMINA	ss3633150161	Oct 12, 2018 (152)
72	ILLUMINA	ss3633858284	Oct 12, 2018 (152)
73	ILLUMINA	ss3634689634	Oct 12, 2018 (152)
74	ILLUMINA	ss3635545850	Oct 12, 2018 (152)
75	ILLUMINA	ss3636378253	Oct 12, 2018 (152)
76	ILLUMINA	ss3637297417	Oct 12, 2018 (152)
77	ILLUMINA	ss3638177044	Oct 12, 2018 (152)
78	ILLUMINA	ss3640396944	Oct 12, 2018 (152)
79	ILLUMINA	ss3641084711	Oct 12, 2018 (152)
80	ILLUMINA	ss3641380213	Oct 12, 2018 (152)
81	OMUKHERJEE_ADBS	ss3646517576	Oct 12, 2018 (152)
82	ILLUMINA	ss3652228043	Oct 12, 2018 (152)
83	EGCUT_WGS	ss3682821648	Jul 13, 2019 (153)
84	EVA_DECODE	ss3700980572	Jul 13, 2019 (153)
85	ILLUMINA	ss3725647367	Jul 13, 2019 (153)
86	ACPOP	ss3742245329	Jul 13, 2019 (153)
87	EVA	ss3754974098	Jul 13, 2019 (153)
88	PAGE_CC	ss3771948931	Jul 13, 2019 (153)
89	KHV_HUMAN_GENOMES	ss3820237750	Jul 13, 2019 (153)
90	SGDP_PRJ	ss3886285268	Apr 27, 2020 (154)
91	KRGDB	ss3936069053	Apr 27, 2020 (154)
92	KOGIC	ss3979361679	Apr 27, 2020 (154)
93	EVA	ss3984727404	Apr 27, 2021 (155)
94	EVA	ss3985805473	Apr 27, 2021 (155)
95	EVA	ss3986076258	Apr 27, 2021 (155)
96	EVA	ss4017780389	Apr 27, 2021 (155)
97	TOPMED	ss5044869724	Apr 27, 2021 (155)
98	TOMMO_GENOMICS	ss5223628488	Apr 27, 2021 (155)
99	1000G_HIGH_COVERAGE	ss5304049666	Oct 16, 2022 (156)
100	EVA	ss5315905796	Oct 16, 2022 (156)
101	EVA	ss5429236297	Oct 16, 2022 (156)
102	HUGCELL_USP	ss5497003328	Oct 16, 2022 (156)
103	EVA	ss5511835256	Oct 16, 2022 (156)
104	1000G_HIGH_COVERAGE	ss5608198266	Oct 16, 2022 (156)
105	SANFORD_IMAGENETICS	ss5660606816	Oct 16, 2022 (156)
106	TOMMO_GENOMICS	ss5780221100	Oct 16, 2022 (156)
107	EVA	ss5799982906	Oct 16, 2022 (156)
108	YY_MCH	ss5816757314	Oct 16, 2022 (156)
109	EVA	ss5834334383	Oct 16, 2022 (156)
110	EVA	ss5847809463	Oct 16, 2022 (156)
111	EVA	ss5851910570	Oct 16, 2022 (156)
112	EVA	ss5914954870	Oct 16, 2022 (156)
113	EVA	ss5952010447	Oct 16, 2022 (156)
114	1000Genomes	NC_000017.10 - 76988192	Oct 12, 2018 (152)
115	1000Genomes_30x	NC_000017.11 - 78992110	Oct 16, 2022 (156)
116	The Avon Longitudinal Study of Parents and Children	NC_000017.10 - 76988192	Oct 12, 2018 (152)
117	Genetic variation in the Estonian population	NC_000017.10 - 76988192	Oct 12, 2018 (152)
118	The Danish reference pan genome	NC_000017.10 - 76988192	Apr 27, 2020 (154)
119	gnomAD - Genomes	NC_000017.11 - 78992110	Apr 27, 2021 (155)
120	Genome of the Netherlands Release 5	NC_000017.10 - 76988192	Apr 27, 2020 (154)
121	HapMap	NC_000017.11 - 78992110	Apr 27, 2020 (154)
122	KOREAN population from KRGDB	NC_000017.10 - 76988192	Apr 27, 2020 (154)
123	Korean Genome Project	NC_000017.11 - 78992110	Apr 27, 2020 (154)
124	Northern Sweden	NC_000017.10 - 76988192	Jul 13, 2019 (153)
125	The PAGE Study	NC_000017.11 - 78992110	Jul 13, 2019 (153)
126	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000017.10 - 76988192	Apr 27, 2021 (155)
127	CNV burdens in cranial meningiomas	NC_000017.10 - 76988192	Apr 27, 2021 (155)
128	Qatari	NC_000017.10 - 76988192	Apr 27, 2020 (154)
129	SGDP_PRJ	NC_000017.10 - 76988192	Apr 27, 2020 (154)
130	Siberian	NC_000017.10 - 76988192	Apr 27, 2020 (154)
131	8.3KJPN	NC_000017.10 - 76988192	Apr 27, 2021 (155)
132	14KJPN	NC_000017.11 - 78992110	Oct 16, 2022 (156)
133	TopMed	NC_000017.11 - 78992110	Apr 27, 2021 (155)
134	UK 10K study - Twins	NC_000017.10 - 76988192	Oct 12, 2018 (152)
135	A Vietnamese Genetic Variation Database	NC_000017.10 - 76988192	Jul 13, 2019 (153)
136	ALFA	NC_000017.11 - 78992110	Apr 27, 2021 (155)
137	ClinVar	RCV000389226.3	Oct 16, 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)
rs2377300	Mar 10, 2006 (126)
rs3211008	Jul 03, 2002 (106)
rs60416571	May 26, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss83670583, ss113883218, ss118138913, ss170321734, ss171768974, ss202825057, ss255808782, ss282854814, ss287221141, ss481077161, ss1697419312, ss1713600696	NC_000017.9:74499786:C:T	NC_000017.11:78992109:C:T	(self)
72951287, 40425135, 28559896, 4456203, 18008073, 43246447, 15530194, 1031400, 276952, 18874269, 38302248, 10192709, 81597795, 40425135, 8934393, ss227674236, ss237334107, ss243611286, ss481099078, ss482092240, ss485333708, ss537285244, ss565427623, ss661242773, ss778550358, ss783112626, ss784069583, ss832371309, ss834007083, ss993367143, ss1081239604, ss1359670076, ss1578258125, ss1636171690, ss1679165723, ss1752242571, ss1936832347, ss1946476273, ss1959774367, ss1968441946, ss2029187877, ss2157676355, ss2629089707, ss2633429503, ss2702243103, ss2710858384, ss2952822371, ss3015958099, ss3021809513, ss3351855711, ss3625719064, ss3627731298, ss3631408580, ss3633150161, ss3633858284, ss3634689634, ss3635545850, ss3636378253, ss3637297417, ss3638177044, ss3640396944, ss3641084711, ss3641380213, ss3646517576, ss3652228043, ss3682821648, ss3742245329, ss3754974098, ss3886285268, ss3936069053, ss3984727404, ss3985805473, ss3986076258, ss4017780389, ss5223628488, ss5315905796, ss5429236297, ss5511835256, ss5660606816, ss5799982906, ss5834334383, ss5847809463, ss5952010447	NC_000017.10:76988191:C:T	NC_000017.11:78992109:C:T	(self)
RCV000389226.3, 95724201, 514761322, 1532436, 35739680, 1170400, 114058204, 260415386, 4191507555, ss2218885777, ss3028417071, ss3700980572, ss3725647367, ss3771948931, ss3820237750, ss3979361679, ss5044869724, ss5304049666, ss5497003328, ss5608198266, ss5780221100, ss5816757314, ss5851910570, ss5914954870	NC_000017.11:78992109:C:T	NC_000017.11:78992109:C:T	(self)
ss19373831	NT_010641.14:10880348:C:T	NC_000017.11:78992109:C:T	(self)
ss13020, ss18193, ss3336757, ss4441764, ss6184861, ss6609880, ss16243667, ss24118740, ss24793372, ss44033020, ss65743149, ss74869323, ss119337473, ss154683238, ss160720801, ss161841322, ss173848511	NT_010783.15:42262343:C:T	NC_000017.11:78992109: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 rs4861

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.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs4861