Name: rs3810414
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.

rs3810414

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr19:1993445 (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: T>C
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.378873 (100284/264690, TOPMED)
C=0.288641 (52487/181842, ALFA)
C=0.364166 (50965/139950, GnomAD) (+ 19 more)
C=0.44980 (35391/78682, PAGE_STUDY)
C=0.41275 (11661/28252, 14KJPN)
C=0.41375 (6932/16754, 8.3KJPN)
C=0.4204 (2692/6404, 1000G_30x)
C=0.4143 (2075/5008, 1000G)
C=0.2763 (1238/4480, Estonian)
C=0.2660 (1025/3854, ALSPAC)
C=0.2780 (1031/3708, TWINSUK)
C=0.3263 (956/2930, KOREAN)
C=0.4297 (813/1892, HapMap)
C=0.3297 (604/1832, Korea1K)
C=0.286 (285/998, GoNL)
C=0.345 (269/780, PRJEB37584)
C=0.293 (176/600, NorthernSweden)
T=0.379 (122/322, SGDP_PRJ)
C=0.412 (89/216, Qatari)
T=0.495 (105/212, Vietnamese)
C=0.35 (14/40, GENOME_DK)
T=0.36 (10/28, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: BTBD2 : 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	186876	T=0.709674	C=0.290326
European	Sub	162802	T=0.726797	C=0.273203
African	Sub	7870	T=0.4543	C=0.5457
African Others	Sub	298	T=0.383	C=0.617
African American	Sub	7572	T=0.4571	C=0.5429
Asian	Sub	708	T=0.614	C=0.386
East Asian	Sub	576	T=0.623	C=0.377
Other Asian	Sub	132	T=0.576	C=0.424
Latin American 1	Sub	750	T=0.641	C=0.359
Latin American 2	Sub	6310	T=0.6552	C=0.3448
South Asian	Sub	190	T=0.674	C=0.326
Other	Sub	8246	T=0.6723	C=0.3277

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	T=0.621127	C=0.378873
Allele Frequency Aggregator	Total	Global	181842	T=0.711359	C=0.288641
Allele Frequency Aggregator	European	Sub	159708	T=0.726770	C=0.273230
Allele Frequency Aggregator	Other	Sub	7446	T=0.6769	C=0.3231
Allele Frequency Aggregator	African	Sub	6730	T=0.4556	C=0.5444
Allele Frequency Aggregator	Latin American 2	Sub	6310	T=0.6552	C=0.3448
Allele Frequency Aggregator	Latin American 1	Sub	750	T=0.641	C=0.359
Allele Frequency Aggregator	Asian	Sub	708	T=0.614	C=0.386
Allele Frequency Aggregator	South Asian	Sub	190	T=0.674	C=0.326
gnomAD - Genomes	Global	Study-wide	139950	T=0.635834	C=0.364166
gnomAD - Genomes	European	Sub	75840	T=0.73638	C=0.26362
gnomAD - Genomes	African	Sub	41914	T=0.45400	C=0.54600
gnomAD - Genomes	American	Sub	13614	T=0.65286	C=0.34714
gnomAD - Genomes	Ashkenazi Jewish	Sub	3320	T=0.6214	C=0.3786
gnomAD - Genomes	East Asian	Sub	3112	T=0.5723	C=0.4277
gnomAD - Genomes	Other	Sub	2150	T=0.6405	C=0.3595
The PAGE Study	Global	Study-wide	78682	T=0.55020	C=0.44980
The PAGE Study	AfricanAmerican	Sub	32506	T=0.46259	C=0.53741
The PAGE Study	Mexican	Sub	10810	T=0.64551	C=0.35449
The PAGE Study	Asian	Sub	8308	T=0.5906	C=0.4094
The PAGE Study	PuertoRican	Sub	7918	T=0.6341	C=0.3659
The PAGE Study	NativeHawaiian	Sub	4534	T=0.4413	C=0.5587
The PAGE Study	Cuban	Sub	4230	T=0.6903	C=0.3097
The PAGE Study	Dominican	Sub	3828	T=0.5867	C=0.4133
The PAGE Study	CentralAmerican	Sub	2450	T=0.6094	C=0.3906
The PAGE Study	SouthAmerican	Sub	1982	T=0.6635	C=0.3365
The PAGE Study	NativeAmerican	Sub	1260	T=0.6587	C=0.3413
The PAGE Study	SouthAsian	Sub	856	T=0.634	C=0.366
14KJPN	JAPANESE	Study-wide	28252	T=0.58725	C=0.41275
8.3KJPN	JAPANESE	Study-wide	16754	T=0.58625	C=0.41375
1000Genomes_30x	Global	Study-wide	6404	T=0.5796	C=0.4204
1000Genomes_30x	African	Sub	1786	T=0.3947	C=0.6053
1000Genomes_30x	Europe	Sub	1266	T=0.7070	C=0.2930
1000Genomes_30x	South Asian	Sub	1202	T=0.6423	C=0.3577
1000Genomes_30x	East Asian	Sub	1170	T=0.5726	C=0.4274
1000Genomes_30x	American	Sub	980	T=0.684	C=0.316
1000Genomes	Global	Study-wide	5008	T=0.5857	C=0.4143
1000Genomes	African	Sub	1322	T=0.4032	C=0.5968
1000Genomes	East Asian	Sub	1008	T=0.5744	C=0.4256
1000Genomes	Europe	Sub	1006	T=0.7177	C=0.2823
1000Genomes	South Asian	Sub	978	T=0.641	C=0.359
1000Genomes	American	Sub	694	T=0.680	C=0.320
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.7237	C=0.2763
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.7340	C=0.2660
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.7220	C=0.2780
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.6737	C=0.3263
HapMap	Global	Study-wide	1892	T=0.5703	C=0.4297
HapMap	American	Sub	770	T=0.625	C=0.375
HapMap	African	Sub	692	T=0.460	C=0.540
HapMap	Asian	Sub	254	T=0.630	C=0.370
HapMap	Europe	Sub	176	T=0.682	C=0.318
Korean Genome Project	KOREAN	Study-wide	1832	T=0.6703	C=0.3297
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.714	C=0.286
CNV burdens in cranial meningiomas	Global	Study-wide	780	T=0.655	C=0.345
CNV burdens in cranial meningiomas	CRM	Sub	780	T=0.655	C=0.345
Northern Sweden	ACPOP	Study-wide	600	T=0.707	C=0.293
SGDP_PRJ	Global	Study-wide	322	T=0.379	C=0.621
Qatari	Global	Study-wide	216	T=0.588	C=0.412
A Vietnamese Genetic Variation Database	Global	Study-wide	212	T=0.495	C=0.505
The Danish reference pan genome	Danish	Study-wide	40	T=0.65	C=0.35
Siberian	Global	Study-wide	28	T=0.36	C=0.64

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 19	NC_000019.10:g.1993445T>C
GRCh37.p13 chr 19	NC_000019.9:g.1993444T>C

Gene: BTBD2, BTB domain containing 2 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
BTBD2 transcript	NM_017797.4:c.528-269A>G	N/A	Intron Variant
BTBD2 transcript variant X1	XM_047439065.1:c.528-269A… XM_047439065.1:c.528-269A>G	N/A	Intron Variant
BTBD2 transcript variant X2	XM_047439066.1:c.84-269A>G	N/A	Intron Variant
BTBD2 transcript variant X3	XM_047439067.1:c.84-269A>G	N/A	Intron Variant
BTBD2 transcript variant X4	XM_047439068.1:c.84-269A>G	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	T=	C
GRCh38.p14 chr 19	NC_000019.10:g.1993445=	NC_000019.10:g.1993445T>C
GRCh37.p13 chr 19	NC_000019.9:g.1993444=	NC_000019.9:g.1993444T>C
BTBD2 transcript	NM_017797.3:c.528-269=	NM_017797.3:c.528-269A>G
BTBD2 transcript	NM_017797.4:c.528-269=	NM_017797.4:c.528-269A>G
BTBD2 transcript variant X1	XM_005259593.1:c.84-269=	XM_005259593.1:c.84-269A>G
BTBD2 transcript variant X1	XM_047439065.1:c.528-269=	XM_047439065.1:c.528-269A>G
BTBD2 transcript variant X2	XM_047439066.1:c.84-269=	XM_047439066.1:c.84-269A>G
BTBD2 transcript variant X3	XM_047439067.1:c.84-269=	XM_047439067.1:c.84-269A>G
BTBD2 transcript variant X4	XM_047439068.1:c.84-269=	XM_047439068.1:c.84-269A>G

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#.

121 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	YUSUKE	ss4996819	Aug 28, 2002 (107)
2	SSAHASNP	ss21550664	Apr 05, 2004 (121)
3	ABI	ss44184063	Mar 14, 2006 (126)
4	ILLUMINA	ss65787034	Oct 16, 2006 (127)
5	PERLEGEN	ss69222346	May 17, 2007 (127)
6	ILLUMINA	ss74878422	Dec 06, 2007 (129)
7	HGSV	ss79921876	Dec 14, 2007 (130)
8	BCMHGSC_JDW	ss90881003	Mar 24, 2008 (129)
9	HUMANGENOME_JCVI	ss96248951	Feb 04, 2009 (130)
10	BGI	ss106041943	Feb 04, 2009 (130)
11	1000GENOMES	ss110982333	Jan 25, 2009 (130)
12	1000GENOMES	ss114740495	Jan 25, 2009 (130)
13	ILLUMINA-UK	ss117617592	Feb 14, 2009 (130)
14	KRIBB_YJKIM	ss119464725	Dec 01, 2009 (131)
15	ENSEMBL	ss136310109	Dec 01, 2009 (131)
16	ENSEMBL	ss137514828	Dec 01, 2009 (131)
17	ILLUMINA	ss160645751	Dec 01, 2009 (131)
18	COMPLETE_GENOMICS	ss167657080	Jul 04, 2010 (132)
19	COMPLETE_GENOMICS	ss168866131	Jul 04, 2010 (132)
20	COMPLETE_GENOMICS	ss171387239	Jul 04, 2010 (132)
21	ILLUMINA	ss173649387	Jul 04, 2010 (132)
22	BUSHMAN	ss203588014	Jul 04, 2010 (132)
23	1000GENOMES	ss228008822	Jul 14, 2010 (132)
24	1000GENOMES	ss237578331	Jul 15, 2010 (132)
25	1000GENOMES	ss243805629	Jul 15, 2010 (132)
26	GMI	ss287333641	Apr 25, 2013 (138)
27	PJP	ss292173544	May 09, 2011 (134)
28	ILLUMINA	ss410930793	Sep 17, 2011 (135)
29	ILLUMINA	ss480845806	May 04, 2012 (137)
30	ILLUMINA	ss480863065	May 04, 2012 (137)
31	ILLUMINA	ss481797774	Sep 08, 2015 (146)
32	ILLUMINA	ss485217790	May 04, 2012 (137)
33	ILLUMINA	ss537198564	Sep 08, 2015 (146)
34	TISHKOFF	ss565808833	Apr 25, 2013 (138)
35	SSMP	ss661661136	Apr 25, 2013 (138)
36	ILLUMINA	ss778897657	Aug 21, 2014 (142)
37	ILLUMINA	ss783054851	Sep 08, 2015 (146)
38	ILLUMINA	ss784013189	Aug 21, 2014 (142)
39	ILLUMINA	ss832312745	Sep 08, 2015 (146)
40	ILLUMINA	ss834358869	Aug 21, 2014 (142)
41	EVA-GONL	ss994013219	Aug 21, 2014 (142)
42	JMKIDD_LAB	ss1081711856	Aug 21, 2014 (142)
43	1000GENOMES	ss1362070053	Aug 21, 2014 (142)
44	DDI	ss1428311834	Apr 01, 2015 (144)
45	EVA_GENOME_DK	ss1578525922	Apr 01, 2015 (144)
46	EVA_UK10K_ALSPAC	ss1637433409	Apr 01, 2015 (144)
47	EVA_UK10K_TWINSUK	ss1680427442	Apr 01, 2015 (144)
48	EVA_DECODE	ss1698076239	Apr 01, 2015 (144)
49	EVA_SVP	ss1713646790	Apr 01, 2015 (144)
50	ILLUMINA	ss1752278121	Sep 08, 2015 (146)
51	HAMMER_LAB	ss1809173422	Sep 08, 2015 (146)
52	WEILL_CORNELL_DGM	ss1937490611	Feb 12, 2016 (147)
53	ILLUMINA	ss1946519510	Feb 12, 2016 (147)
54	ILLUMINA	ss1959828140	Feb 12, 2016 (147)
55	GENOMED	ss1968592899	Jul 19, 2016 (147)
56	JJLAB	ss2029520312	Sep 14, 2016 (149)
57	USC_VALOUEV	ss2158032886	Dec 20, 2016 (150)
58	HUMAN_LONGEVITY	ss2223719847	Dec 20, 2016 (150)
59	SYSTEMSBIOZJU	ss2629258834	Nov 08, 2017 (151)
60	ILLUMINA	ss2633509131	Nov 08, 2017 (151)
61	GRF	ss2702636518	Nov 08, 2017 (151)
62	ILLUMINA	ss2710874671	Nov 08, 2017 (151)
63	GNOMAD	ss2959624501	Nov 08, 2017 (151)
64	SWEGEN	ss3016964278	Nov 08, 2017 (151)
65	ILLUMINA	ss3021868738	Nov 08, 2017 (151)
66	BIOINF_KMB_FNS_UNIBA	ss3028592676	Nov 08, 2017 (151)
67	CSHL	ss3352161019	Nov 08, 2017 (151)
68	ILLUMINA	ss3625730475	Oct 12, 2018 (152)
69	ILLUMINA	ss3627871772	Oct 12, 2018 (152)
70	ILLUMINA	ss3631483446	Oct 12, 2018 (152)
71	ILLUMINA	ss3633172421	Oct 12, 2018 (152)
72	ILLUMINA	ss3633881819	Oct 12, 2018 (152)
73	ILLUMINA	ss3634718589	Oct 12, 2018 (152)
74	ILLUMINA	ss3635568883	Oct 12, 2018 (152)
75	ILLUMINA	ss3636409230	Oct 12, 2018 (152)
76	ILLUMINA	ss3637320549	Oct 12, 2018 (152)
77	ILLUMINA	ss3638211317	Oct 12, 2018 (152)
78	ILLUMINA	ss3640425897	Oct 12, 2018 (152)
79	ILLUMINA	ss3643185967	Oct 12, 2018 (152)
80	ILLUMINA	ss3644712061	Oct 12, 2018 (152)
81	URBANLAB	ss3650852450	Oct 12, 2018 (152)
82	ILLUMINA	ss3652292715	Oct 12, 2018 (152)
83	EGCUT_WGS	ss3683813187	Jul 13, 2019 (153)
84	EVA_DECODE	ss3702189635	Jul 13, 2019 (153)
85	ILLUMINA	ss3725698716	Jul 13, 2019 (153)
86	ACPOP	ss3742788499	Jul 13, 2019 (153)
87	ILLUMINA	ss3744162700	Jul 13, 2019 (153)
88	ILLUMINA	ss3745018661	Jul 13, 2019 (153)
89	EVA	ss3755724488	Jul 13, 2019 (153)
90	PAGE_CC	ss3771989574	Jul 13, 2019 (153)
91	ILLUMINA	ss3772516079	Jul 13, 2019 (153)
92	KHV_HUMAN_GENOMES	ss3820978466	Jul 13, 2019 (153)
93	EVA	ss3835311400	Apr 27, 2020 (154)
94	EVA	ss3841278276	Apr 27, 2020 (154)
95	EVA	ss3846782123	Apr 27, 2020 (154)
96	SGDP_PRJ	ss3887597047	Apr 27, 2020 (154)
97	KRGDB	ss3937525733	Apr 27, 2020 (154)
98	KOGIC	ss3980653796	Apr 27, 2020 (154)
99	EVA	ss3984737264	Apr 25, 2021 (155)
100	EVA	ss4017812114	Apr 25, 2021 (155)
101	TOPMED	ss5065670344	Apr 25, 2021 (155)
102	TOMMO_GENOMICS	ss5226369422	Apr 25, 2021 (155)
103	1000G_HIGH_COVERAGE	ss5306220458	Oct 16, 2022 (156)
104	EVA	ss5315956125	Oct 16, 2022 (156)
105	EVA	ss5433110227	Oct 16, 2022 (156)
106	HUGCELL_USP	ss5498891109	Oct 16, 2022 (156)
107	EVA	ss5512028027	Oct 16, 2022 (156)
108	1000G_HIGH_COVERAGE	ss5611516174	Oct 16, 2022 (156)
109	SANFORD_IMAGENETICS	ss5624422023	Oct 16, 2022 (156)
110	SANFORD_IMAGENETICS	ss5661829415	Oct 16, 2022 (156)
111	TOMMO_GENOMICS	ss5784517150	Oct 16, 2022 (156)
112	EVA	ss5800002004	Oct 16, 2022 (156)
113	YY_MCH	ss5817339771	Oct 16, 2022 (156)
114	EVA	ss5840150246	Oct 16, 2022 (156)
115	EVA	ss5847492101	Oct 16, 2022 (156)
116	EVA	ss5847830818	Oct 16, 2022 (156)
117	EVA	ss5852175017	Oct 16, 2022 (156)
118	EVA	ss5927016747	Oct 16, 2022 (156)
119	EVA	ss5953260417	Oct 16, 2022 (156)
120	EVA	ss5979536896	Oct 16, 2022 (156)
121	EVA	ss5981023308	Oct 16, 2022 (156)
122	1000Genomes	NC_000019.9 - 1993444	Oct 12, 2018 (152)
123	1000Genomes_30x	NC_000019.10 - 1993445	Oct 16, 2022 (156)
124	The Avon Longitudinal Study of Parents and Children	NC_000019.9 - 1993444	Oct 12, 2018 (152)
125	Genetic variation in the Estonian population	NC_000019.9 - 1993444	Oct 12, 2018 (152)
126	The Danish reference pan genome	NC_000019.9 - 1993444	Apr 27, 2020 (154)
127	gnomAD - Genomes	NC_000019.10 - 1993445	Apr 25, 2021 (155)
128	Genome of the Netherlands Release 5	NC_000019.9 - 1993444	Apr 27, 2020 (154)
129	HapMap	NC_000019.10 - 1993445	Apr 27, 2020 (154)
130	KOREAN population from KRGDB	NC_000019.9 - 1993444	Apr 27, 2020 (154)
131	Korean Genome Project	NC_000019.10 - 1993445	Apr 27, 2020 (154)
132	Northern Sweden	NC_000019.9 - 1993444	Jul 13, 2019 (153)
133	The PAGE Study	NC_000019.10 - 1993445	Jul 13, 2019 (153)
134	CNV burdens in cranial meningiomas	NC_000019.9 - 1993444	Apr 25, 2021 (155)
135	Qatari	NC_000019.9 - 1993444	Apr 27, 2020 (154)
136	SGDP_PRJ	NC_000019.9 - 1993444	Apr 27, 2020 (154)
137	Siberian	NC_000019.9 - 1993444	Apr 27, 2020 (154)
138	8.3KJPN	NC_000019.9 - 1993444	Apr 25, 2021 (155)
139	14KJPN	NC_000019.10 - 1993445	Oct 16, 2022 (156)
140	TopMed	NC_000019.10 - 1993445	Apr 25, 2021 (155)
141	UK 10K study - Twins	NC_000019.9 - 1993444	Oct 12, 2018 (152)
142	A Vietnamese Genetic Variation Database	NC_000019.9 - 1993444	Jul 13, 2019 (153)
143	ALFA	NC_000019.10 - 1993445	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)
rs57276971	May 23, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss79921876, ss90881003, ss110982333, ss114740495, ss117617592, ss160645751, ss167657080, ss168866131, ss171387239, ss203588014, ss287333641, ss292173544, ss480845806, ss1698076239, ss1713646790, ss3643185967	NC_000019.8:1944443:T:C	NC_000019.10:1993444:T:C	(self)
75436616, 41812634, 29551435, 4713060, 18628603, 44703127, 16073364, 286816, 19532533, 39614027, 10549240, 84338729, 41812634, 9246817, ss228008822, ss237578331, ss243805629, ss480863065, ss481797774, ss485217790, ss537198564, ss565808833, ss661661136, ss778897657, ss783054851, ss784013189, ss832312745, ss834358869, ss994013219, ss1081711856, ss1362070053, ss1428311834, ss1578525922, ss1637433409, ss1680427442, ss1752278121, ss1809173422, ss1937490611, ss1946519510, ss1959828140, ss1968592899, ss2029520312, ss2158032886, ss2629258834, ss2633509131, ss2702636518, ss2710874671, ss2959624501, ss3016964278, ss3021868738, ss3352161019, ss3625730475, ss3627871772, ss3631483446, ss3633172421, ss3633881819, ss3634718589, ss3635568883, ss3636409230, ss3637320549, ss3638211317, ss3640425897, ss3644712061, ss3652292715, ss3683813187, ss3742788499, ss3744162700, ss3745018661, ss3755724488, ss3772516079, ss3835311400, ss3841278276, ss3887597047, ss3937525733, ss3984737264, ss4017812114, ss5226369422, ss5315956125, ss5433110227, ss5512028027, ss5624422023, ss5661829415, ss5800002004, ss5840150246, ss5847492101, ss5847830818, ss5953260417, ss5979536896, ss5981023308	NC_000019.9:1993443:T:C	NC_000019.10:1993444:T:C	(self)
99042109, 531995398, 1658862, 37031797, 1211043, 118354254, 281216008, 677838099, ss2223719847, ss3028592676, ss3650852450, ss3702189635, ss3725698716, ss3771989574, ss3820978466, ss3846782123, ss3980653796, ss5065670344, ss5306220458, ss5498891109, ss5611516174, ss5784517150, ss5817339771, ss5852175017, ss5927016747	NC_000019.10:1993444:T:C	NC_000019.10:1993444:T:C	(self)
ss4996819, ss21550664, ss44184063, ss65787034, ss69222346, ss74878422, ss96248951, ss106041943, ss119464725, ss136310109, ss137514828, ss173649387, ss410930793	NT_011255.14:1933443:T:C	NC_000019.10:1993444:T: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 rs3810414

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

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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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs3810414