Name: rs4816416
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.

rs4816416

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr21:14877609 (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=0.123087 (32580/264690, TOPMED)
T=0.158039 (32410/205076, GENOGRAPHIC)
T=0.156648 (31934/203858, ALFA) (+ 21 more)
T=0.120180 (16836/140090, GnomAD)
T=0.10737 (3034/28258, 14KJPN)
T=0.10662 (1787/16760, 8.3KJPN)
T=0.1037 (664/6404, 1000G_30x)
T=0.1040 (521/5008, 1000G)
T=0.1127 (505/4480, Estonian)
T=0.1614 (622/3854, ALSPAC)
T=0.1615 (599/3708, TWINSUK)
T=0.0773 (226/2922, KOREAN)
T=0.1483 (309/2084, HGDP_Stanford)
T=0.0876 (165/1884, HapMap)
T=0.1813 (206/1136, Daghestan)
T=0.149 (149/998, GoNL)
T=0.127 (76/600, NorthernSweden)
T=0.245 (53/216, Qatari)
T=0.061 (13/214, Vietnamese)
C=0.476 (59/124, SGDP_PRJ)
T=0.12 (8/68, Ancient Sardinia)
T=0.15 (6/40, GENOME_DK)
C=0.5 (3/6, Siberian)
T=0.5 (3/6, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LINC02246 : 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	203952	C=0.843336	T=0.156664
European	Sub	173834	C=0.838754	T=0.161246
African	Sub	9692	C=0.9552	T=0.0448
African Others	Sub	346	C=0.983	T=0.017
African American	Sub	9346	C=0.9542	T=0.0458
Asian	Sub	700	C=0.947	T=0.053
East Asian	Sub	554	C=0.951	T=0.049
Other Asian	Sub	146	C=0.932	T=0.068
Latin American 1	Sub	840	C=0.879	T=0.121
Latin American 2	Sub	6894	C=0.7955	T=0.2045
South Asian	Sub	5044	C=0.8352	T=0.1648
Other	Sub	6948	C=0.8405	T=0.1595

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	C=0.876913	T=0.123087
Genographic Project	Global	Study-wide	205076	C=0.841961	T=0.158039
Allele Frequency Aggregator	Total	Global	203858	C=0.843352	T=0.156648
Allele Frequency Aggregator	European	Sub	173758	C=0.838770	T=0.161230
Allele Frequency Aggregator	African	Sub	9692	C=0.9552	T=0.0448
Allele Frequency Aggregator	Other	Sub	6930	C=0.8405	T=0.1595
Allele Frequency Aggregator	Latin American 2	Sub	6894	C=0.7955	T=0.2045
Allele Frequency Aggregator	South Asian	Sub	5044	C=0.8352	T=0.1648
Allele Frequency Aggregator	Latin American 1	Sub	840	C=0.879	T=0.121
Allele Frequency Aggregator	Asian	Sub	700	C=0.947	T=0.053
gnomAD - Genomes	Global	Study-wide	140090	C=0.879820	T=0.120180
gnomAD - Genomes	European	Sub	75884	C=0.85007	T=0.14993
gnomAD - Genomes	African	Sub	41990	C=0.95530	T=0.04470
gnomAD - Genomes	American	Sub	13632	C=0.82526	T=0.17474
gnomAD - Genomes	Ashkenazi Jewish	Sub	3304	C=0.7691	T=0.2309
gnomAD - Genomes	East Asian	Sub	3132	C=0.9527	T=0.0473
gnomAD - Genomes	Other	Sub	2148	C=0.8655	T=0.1345
14KJPN	JAPANESE	Study-wide	28258	C=0.89263	T=0.10737
8.3KJPN	JAPANESE	Study-wide	16760	C=0.89338	T=0.10662
1000Genomes_30x	Global	Study-wide	6404	C=0.8963	T=0.1037
1000Genomes_30x	African	Sub	1786	C=0.9776	T=0.0224
1000Genomes_30x	Europe	Sub	1266	C=0.8468	T=0.1532
1000Genomes_30x	South Asian	Sub	1202	C=0.8461	T=0.1539
1000Genomes_30x	East Asian	Sub	1170	C=0.9504	T=0.0496
1000Genomes_30x	American	Sub	980	C=0.809	T=0.191
1000Genomes	Global	Study-wide	5008	C=0.8960	T=0.1040
1000Genomes	African	Sub	1322	C=0.9781	T=0.0219
1000Genomes	East Asian	Sub	1008	C=0.9464	T=0.0536
1000Genomes	Europe	Sub	1006	C=0.8400	T=0.1600
1000Genomes	South Asian	Sub	978	C=0.851	T=0.149
1000Genomes	American	Sub	694	C=0.811	T=0.189
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.8873	T=0.1127
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.8386	T=0.1614
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.8385	T=0.1615
KOREAN population from KRGDB	KOREAN	Study-wide	2922	C=0.9227	T=0.0773
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	C=0.8517	T=0.1483
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	C=0.947	T=0.053
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	C=0.826	T=0.174
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	C=0.811	T=0.189
HGDP-CEPH-db Supplement 1	Europe	Sub	320	C=0.816	T=0.184
HGDP-CEPH-db Supplement 1	Africa	Sub	242	C=0.979	T=0.021
HGDP-CEPH-db Supplement 1	America	Sub	216	C=0.648	T=0.352
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	C=0.92	T=0.08
HapMap	Global	Study-wide	1884	C=0.9124	T=0.0876
HapMap	American	Sub	768	C=0.888	T=0.112
HapMap	African	Sub	686	C=0.980	T=0.020
HapMap	Asian	Sub	254	C=0.909	T=0.091
HapMap	Europe	Sub	176	C=0.761	T=0.239
Genome-wide autozygosity in Daghestan	Global	Study-wide	1136	C=0.8187	T=0.1813
Genome-wide autozygosity in Daghestan	Daghestan	Sub	628	C=0.823	T=0.177
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	C=0.812	T=0.188
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	C=0.861	T=0.139
Genome-wide autozygosity in Daghestan	Europe	Sub	108	C=0.787	T=0.213
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	C=0.84	T=0.16
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=0.851	T=0.149
Northern Sweden	ACPOP	Study-wide	600	C=0.873	T=0.127
Qatari	Global	Study-wide	216	C=0.755	T=0.245
A Vietnamese Genetic Variation Database	Global	Study-wide	214	C=0.939	T=0.061
SGDP_PRJ	Global	Study-wide	124	C=0.476	T=0.524
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	68	C=0.88	T=0.12
The Danish reference pan genome	Danish	Study-wide	40	C=0.85	T=0.15
Siberian	Global	Study-wide	6	C=0.5	T=0.5

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 21	NC_000021.9:g.14877609C>T
GRCh37.p13 chr 21	NC_000021.8:g.16249930C>T

Gene: LINC02246, long intergenic non-protein coding RNA 2246 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ASMER1 transcript	NR_146322.1: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=	T
GRCh38.p14 chr 21	NC_000021.9:g.14877609=	NC_000021.9:g.14877609C>T
GRCh37.p13 chr 21	NC_000021.8:g.16249930=	NC_000021.8:g.16249930C>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#.

116 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	WI_SSAHASNP	ss6649035	Feb 20, 2003 (111)
2	PERLEGEN	ss14866783	Dec 05, 2003 (119)
3	ABI	ss44286537	Mar 13, 2006 (126)
4	AFFY	ss66007882	Nov 30, 2006 (127)
5	ILLUMINA	ss66749745	Nov 30, 2006 (127)
6	ILLUMINA	ss67381890	Nov 30, 2006 (127)
7	ILLUMINA	ss67759618	Nov 30, 2006 (127)
8	PERLEGEN	ss69248296	May 17, 2007 (127)
9	ILLUMINA	ss70827598	May 26, 2008 (130)
10	ILLUMINA	ss71409862	May 17, 2007 (127)
11	ILLUMINA	ss75720901	Dec 07, 2007 (129)
12	ILLUMINA	ss79197013	Dec 15, 2007 (130)
13	KRIBB_YJKIM	ss84363959	Dec 15, 2007 (130)
14	HUMANGENOME_JCVI	ss96155804	Feb 06, 2009 (130)
15	1000GENOMES	ss112274060	Jan 25, 2009 (130)
16	ILLUMINA	ss122398196	Dec 01, 2009 (131)
17	ENSEMBL	ss135651089	Dec 01, 2009 (131)
18	ILLUMINA	ss154320075	Dec 01, 2009 (131)
19	ILLUMINA	ss159496735	Dec 01, 2009 (131)
20	ILLUMINA	ss160715764	Dec 01, 2009 (131)
21	ILLUMINA	ss171931586	Jul 04, 2010 (132)
22	ILLUMINA	ss173827953	Jul 04, 2010 (132)
23	BCM-HGSC-SUB	ss208782562	Jul 04, 2010 (132)
24	1000GENOMES	ss228460706	Jul 14, 2010 (132)
25	1000GENOMES	ss237909866	Jul 15, 2010 (132)
26	1000GENOMES	ss244063014	Jul 15, 2010 (132)
27	GMI	ss283469913	May 04, 2012 (137)
28	GMI	ss287496899	Apr 25, 2013 (138)
29	PJP	ss292676527	May 09, 2011 (134)
30	ILLUMINA	ss481060954	May 04, 2012 (137)
31	ILLUMINA	ss481082720	May 04, 2012 (137)
32	ILLUMINA	ss482077213	Sep 08, 2015 (146)
33	ILLUMINA	ss485325520	May 04, 2012 (137)
34	ILLUMINA	ss537278798	Sep 08, 2015 (146)
35	TISHKOFF	ss566379829	Apr 25, 2013 (138)
36	SSMP	ss662285698	Apr 25, 2013 (138)
37	ILLUMINA	ss779059307	Sep 08, 2015 (146)
38	ILLUMINA	ss783108570	Sep 08, 2015 (146)
39	ILLUMINA	ss784065627	Sep 08, 2015 (146)
40	ILLUMINA	ss825527531	Apr 01, 2015 (144)
41	ILLUMINA	ss832367219	Sep 08, 2015 (146)
42	ILLUMINA	ss833008112	Jul 13, 2019 (153)
43	ILLUMINA	ss834522451	Sep 08, 2015 (146)
44	EVA-GONL	ss994931775	Aug 21, 2014 (142)
45	JMKIDD_LAB	ss1082351399	Aug 21, 2014 (142)
46	1000GENOMES	ss1365602091	Aug 21, 2014 (142)
47	HAMMER_LAB	ss1397774453	Sep 08, 2015 (146)
48	DDI	ss1429127379	Apr 01, 2015 (144)
49	EVA_GENOME_DK	ss1579587781	Apr 01, 2015 (144)
50	EVA_UK10K_ALSPAC	ss1639196082	Apr 01, 2015 (144)
51	EVA_UK10K_TWINSUK	ss1682190115	Apr 01, 2015 (144)
52	EVA_DECODE	ss1698995132	Apr 01, 2015 (144)
53	EVA_SVP	ss1713709873	Apr 01, 2015 (144)
54	ILLUMINA	ss1752400132	Sep 08, 2015 (146)
55	WEILL_CORNELL_DGM	ss1938483910	Feb 12, 2016 (147)
56	GENOMED	ss1969178558	Jul 19, 2016 (147)
57	JJLAB	ss2030011452	Sep 14, 2016 (149)
58	USC_VALOUEV	ss2158610658	Dec 20, 2016 (150)
59	HUMAN_LONGEVITY	ss2244373007	Dec 20, 2016 (150)
60	ILLUMINA	ss2633827069	Nov 08, 2017 (151)
61	GRF	ss2704333230	Nov 08, 2017 (151)
62	GNOMAD	ss2969886909	Nov 08, 2017 (151)
63	AFFY	ss2985223715	Nov 08, 2017 (151)
64	AFFY	ss2985840731	Nov 08, 2017 (151)
65	SWEGEN	ss3018612219	Nov 08, 2017 (151)
66	BIOINF_KMB_FNS_UNIBA	ss3028840472	Nov 08, 2017 (151)
67	CSHL	ss3352635492	Nov 08, 2017 (151)
68	ILLUMINA	ss3628442039	Oct 12, 2018 (152)
69	ILLUMINA	ss3631781637	Oct 12, 2018 (152)
70	ILLUMINA	ss3633258681	Oct 12, 2018 (152)
71	ILLUMINA	ss3633973387	Oct 12, 2018 (152)
72	ILLUMINA	ss3634846977	Oct 12, 2018 (152)
73	ILLUMINA	ss3635658267	Oct 12, 2018 (152)
74	ILLUMINA	ss3636541303	Oct 12, 2018 (152)
75	ILLUMINA	ss3637410414	Oct 12, 2018 (152)
76	ILLUMINA	ss3638358505	Oct 12, 2018 (152)
77	ILLUMINA	ss3639182543	Oct 12, 2018 (152)
78	ILLUMINA	ss3639605960	Oct 12, 2018 (152)
79	ILLUMINA	ss3640554275	Oct 12, 2018 (152)
80	ILLUMINA	ss3641131364	Oct 12, 2018 (152)
81	ILLUMINA	ss3641427662	Oct 12, 2018 (152)
82	ILLUMINA	ss3643320346	Oct 12, 2018 (152)
83	URBANLAB	ss3651075681	Oct 12, 2018 (152)
84	ILLUMINA	ss3653991882	Oct 12, 2018 (152)
85	EGCUT_WGS	ss3685182523	Jul 13, 2019 (153)
86	EVA_DECODE	ss3707388402	Jul 13, 2019 (153)
87	ACPOP	ss3743574790	Jul 13, 2019 (153)
88	ILLUMINA	ss3745146863	Jul 13, 2019 (153)
89	EVA	ss3758896953	Jul 13, 2019 (153)
90	ILLUMINA	ss3772642954	Jul 13, 2019 (153)
91	PACBIO	ss3788713141	Jul 13, 2019 (153)
92	PACBIO	ss3793593846	Jul 13, 2019 (153)
93	PACBIO	ss3798479978	Jul 13, 2019 (153)
94	KHV_HUMAN_GENOMES	ss3822054780	Jul 13, 2019 (153)
95	EVA	ss3835778013	Apr 27, 2020 (154)
96	HGDP	ss3847674636	Apr 27, 2020 (154)
97	SGDP_PRJ	ss3889634114	Apr 27, 2020 (154)
98	KRGDB	ss3940043022	Apr 27, 2020 (154)
99	EVA	ss3985892696	Apr 27, 2021 (155)
100	EVA	ss4017859096	Apr 27, 2021 (155)
101	TOPMED	ss5095643467	Apr 27, 2021 (155)
102	TOMMO_GENOMICS	ss5230768246	Apr 27, 2021 (155)
103	1000G_HIGH_COVERAGE	ss5309612057	Oct 13, 2022 (156)
104	GENOGRAPHIC	ss5314582359	Oct 13, 2022 (156)
105	EVA	ss5316024581	Oct 13, 2022 (156)
106	EVA	ss5438803638	Oct 13, 2022 (156)
107	HUGCELL_USP	ss5501714275	Oct 13, 2022 (156)
108	1000G_HIGH_COVERAGE	ss5616456831	Oct 13, 2022 (156)
109	SANFORD_IMAGENETICS	ss5663656887	Oct 13, 2022 (156)
110	TOMMO_GENOMICS	ss5791072066	Oct 13, 2022 (156)
111	EVA	ss5800028547	Oct 13, 2022 (156)
112	YY_MCH	ss5818292430	Oct 13, 2022 (156)
113	EVA	ss5838804643	Oct 13, 2022 (156)
114	EVA	ss5853225104	Oct 13, 2022 (156)
115	EVA	ss5891663873	Oct 13, 2022 (156)
116	EVA	ss5958542191	Oct 13, 2022 (156)
117	1000Genomes	NC_000021.8 - 16249930	Oct 12, 2018 (152)
118	1000Genomes_30x	NC_000021.9 - 14877609	Oct 13, 2022 (156)
119	The Avon Longitudinal Study of Parents and Children	NC_000021.8 - 16249930	Oct 12, 2018 (152)
120	Genome-wide autozygosity in Daghestan	NC_000021.7 - 15171801	Apr 27, 2020 (154)
121	Genetic variation in the Estonian population	NC_000021.8 - 16249930	Oct 12, 2018 (152)
122	Genographic Project	NC_000021.9 - 14877609	Oct 13, 2022 (156)
123	The Danish reference pan genome	NC_000021.8 - 16249930	Apr 27, 2020 (154)
124	gnomAD - Genomes	NC_000021.9 - 14877609	Apr 27, 2021 (155)
125	Genome of the Netherlands Release 5	NC_000021.8 - 16249930	Apr 27, 2020 (154)
126	HGDP-CEPH-db Supplement 1	NC_000021.7 - 15171801	Apr 27, 2020 (154)
127	HapMap	NC_000021.9 - 14877609	Apr 27, 2020 (154)
128	KOREAN population from KRGDB	NC_000021.8 - 16249930	Apr 27, 2020 (154)
129	Northern Sweden	NC_000021.8 - 16249930	Jul 13, 2019 (153)
130	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000021.8 - 16249930	Apr 27, 2021 (155)
131	Qatari	NC_000021.8 - 16249930	Apr 27, 2020 (154)
132	SGDP_PRJ	NC_000021.8 - 16249930	Apr 27, 2020 (154)
133	Siberian	NC_000021.8 - 16249930	Apr 27, 2020 (154)
134	8.3KJPN	NC_000021.8 - 16249930	Apr 27, 2021 (155)
135	14KJPN	NC_000021.9 - 14877609	Oct 13, 2022 (156)
136	TopMed	NC_000021.9 - 14877609	Apr 27, 2021 (155)
137	UK 10K study - Twins	NC_000021.8 - 16249930	Oct 12, 2018 (152)
138	A Vietnamese Genetic Variation Database	NC_000021.8 - 16249930	Jul 13, 2019 (153)
139	ALFA	NC_000021.9 - 14877609	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)
rs60597667	May 26, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
288526, 352528, ss112274060, ss208782562, ss283469913, ss287496899, ss292676527, ss481060954, ss825527531, ss1397774453, ss1698995132, ss1713709873, ss3639182543, ss3639605960, ss3643320346, ss3847674636	NC_000021.7:15171800:C:T	NC_000021.9:14877608:C:T	(self)
79093826, 43765258, 30920771, 5752720, 19494449, 47220416, 16859655, 1118623, 20525832, 41651094, 11127012, 88737553, 43765258, 9651124, ss228460706, ss237909866, ss244063014, ss481082720, ss482077213, ss485325520, ss537278798, ss566379829, ss662285698, ss779059307, ss783108570, ss784065627, ss832367219, ss833008112, ss834522451, ss994931775, ss1082351399, ss1365602091, ss1429127379, ss1579587781, ss1639196082, ss1682190115, ss1752400132, ss1938483910, ss1969178558, ss2030011452, ss2158610658, ss2633827069, ss2704333230, ss2969886909, ss2985223715, ss2985840731, ss3018612219, ss3352635492, ss3628442039, ss3631781637, ss3633258681, ss3633973387, ss3634846977, ss3635658267, ss3636541303, ss3637410414, ss3638358505, ss3640554275, ss3641131364, ss3641427662, ss3653991882, ss3685182523, ss3743574790, ss3745146863, ss3758896953, ss3772642954, ss3788713141, ss3793593846, ss3798479978, ss3835778013, ss3889634114, ss3940043022, ss3985892696, ss4017859096, ss5230768246, ss5316024581, ss5438803638, ss5663656887, ss5800028547, ss5838804643, ss5958542191	NC_000021.8:16249929:C:T	NC_000021.9:14877608:C:T	(self)
103982766, 95557, 558336933, 2173189, 124909170, 370752413, 3695787128, ss2244373007, ss3028840472, ss3651075681, ss3707388402, ss3822054780, ss5095643467, ss5309612057, ss5314582359, ss5501714275, ss5616456831, ss5791072066, ss5818292430, ss5853225104, ss5891663873	NC_000021.9:14877608:C:T	NC_000021.9:14877608:C:T	(self)
ss6649035, ss14866783, ss44286537, ss66007882, ss66749745, ss67381890, ss67759618, ss69248296, ss70827598, ss71409862, ss75720901, ss79197013, ss84363959, ss96155804, ss122398196, ss135651089, ss154320075, ss159496735, ss160715764, ss171931586, ss173827953	NT_011512.11:1911800:C:T	NC_000021.9:14877608: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 rs4816416

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

rs4816416