Name: rs10845411
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.

rs10845411

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr12:11789499 (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: G>C
Variation Type: SNV Single Nucleotide Variation
Frequency: G=0.076089 (20140/264690, TOPMED)
G=0.080661 (11305/140154, GnomAD)
G=0.06259 (4926/78700, PAGE_STUDY) (+ 17 more)
G=0.08585 (2426/28258, 14KJPN)
G=0.09084 (1716/18890, ALFA)
G=0.08705 (1459/16760, 8.3KJPN)
G=0.0762 (488/6404, 1000G_30x)
G=0.0709 (355/5008, 1000G)
G=0.1335 (598/4480, Estonian)
G=0.0833 (321/3854, ALSPAC)
G=0.0793 (294/3708, TWINSUK)
G=0.1065 (312/2930, KOREAN)
G=0.1250 (142/1136, Daghestan)
G=0.080 (80/998, GoNL)
G=0.082 (49/600, NorthernSweden)
G=0.068 (38/556, SGDP_PRJ)
G=0.055 (18/330, HapMap)
G=0.079 (17/216, Qatari)
G=0.04 (2/54, Siberian)
G=0.10 (4/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ETV6 : 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	18890	G=0.09084	C=0.90916
European	Sub	14286	G=0.10549	C=0.89451
African	Sub	2946	G=0.0387	C=0.9613
African Others	Sub	114	G=0.026	C=0.974
African American	Sub	2832	G=0.0392	C=0.9608
Asian	Sub	112	G=0.062	C=0.938
East Asian	Sub	86	G=0.07	C=0.93
Other Asian	Sub	26	G=0.04	C=0.96
Latin American 1	Sub	146	G=0.082	C=0.918
Latin American 2	Sub	610	G=0.046	C=0.954
South Asian	Sub	98	G=0.07	C=0.93
Other	Sub	692	G=0.059	C=0.941

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	G=0.076089	C=0.923911
gnomAD - Genomes	Global	Study-wide	140154	G=0.080661	C=0.919339
gnomAD - Genomes	European	Sub	75906	G=0.09582	C=0.90418
gnomAD - Genomes	African	Sub	41988	G=0.05161	C=0.94839
gnomAD - Genomes	American	Sub	13654	G=0.06386	C=0.93614
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	G=0.1376	C=0.8624
gnomAD - Genomes	East Asian	Sub	3134	G=0.1110	C=0.8890
gnomAD - Genomes	Other	Sub	2150	G=0.0874	C=0.9126
The PAGE Study	Global	Study-wide	78700	G=0.06259	C=0.93741
The PAGE Study	AfricanAmerican	Sub	32516	G=0.05225	C=0.94775
The PAGE Study	Mexican	Sub	10810	G=0.04940	C=0.95060
The PAGE Study	Asian	Sub	8318	G=0.0843	C=0.9157
The PAGE Study	PuertoRican	Sub	7918	G=0.0962	C=0.9038
The PAGE Study	NativeHawaiian	Sub	4532	G=0.0503	C=0.9497
The PAGE Study	Cuban	Sub	4230	G=0.0853	C=0.9147
The PAGE Study	Dominican	Sub	3828	G=0.0747	C=0.9253
The PAGE Study	CentralAmerican	Sub	2450	G=0.0461	C=0.9539
The PAGE Study	SouthAmerican	Sub	1982	G=0.0494	C=0.9506
The PAGE Study	NativeAmerican	Sub	1260	G=0.0627	C=0.9373
The PAGE Study	SouthAsian	Sub	856	G=0.076	C=0.924
14KJPN	JAPANESE	Study-wide	28258	G=0.08585	C=0.91415
Allele Frequency Aggregator	Total	Global	18890	G=0.09084	C=0.90916
Allele Frequency Aggregator	European	Sub	14286	G=0.10549	C=0.89451
Allele Frequency Aggregator	African	Sub	2946	G=0.0387	C=0.9613
Allele Frequency Aggregator	Other	Sub	692	G=0.059	C=0.941
Allele Frequency Aggregator	Latin American 2	Sub	610	G=0.046	C=0.954
Allele Frequency Aggregator	Latin American 1	Sub	146	G=0.082	C=0.918
Allele Frequency Aggregator	Asian	Sub	112	G=0.062	C=0.938
Allele Frequency Aggregator	South Asian	Sub	98	G=0.07	C=0.93
8.3KJPN	JAPANESE	Study-wide	16760	G=0.08705	C=0.91295
1000Genomes_30x	Global	Study-wide	6404	G=0.0762	C=0.9238
1000Genomes_30x	African	Sub	1786	G=0.0392	C=0.9608
1000Genomes_30x	Europe	Sub	1266	G=0.0964	C=0.9036
1000Genomes_30x	South Asian	Sub	1202	G=0.0882	C=0.9118
1000Genomes_30x	East Asian	Sub	1170	G=0.0949	C=0.9051
1000Genomes_30x	American	Sub	980	G=0.081	C=0.919
1000Genomes	Global	Study-wide	5008	G=0.0709	C=0.9291
1000Genomes	African	Sub	1322	G=0.0408	C=0.9592
1000Genomes	East Asian	Sub	1008	G=0.0784	C=0.9216
1000Genomes	Europe	Sub	1006	G=0.0905	C=0.9095
1000Genomes	South Asian	Sub	978	G=0.082	C=0.918
1000Genomes	American	Sub	694	G=0.073	C=0.927
Genetic variation in the Estonian population	Estonian	Study-wide	4480	G=0.1335	C=0.8665
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.0833	C=0.9167
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.0793	C=0.9207
KOREAN population from KRGDB	KOREAN	Study-wide	2930	G=0.1065	C=0.8935
Genome-wide autozygosity in Daghestan	Global	Study-wide	1136	G=0.1250	C=0.8750
Genome-wide autozygosity in Daghestan	Daghestan	Sub	628	G=0.131	C=0.869
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	G=0.111	C=0.889
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	G=0.180	C=0.820
Genome-wide autozygosity in Daghestan	Europe	Sub	108	G=0.120	C=0.880
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	G=0.06	C=0.94
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	G=0.08	C=0.92
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	G=0.080	C=0.920
Northern Sweden	ACPOP	Study-wide	600	G=0.082	C=0.918
SGDP_PRJ	Global	Study-wide	556	G=0.068	C=0.932
HapMap	Global	Study-wide	330	G=0.055	C=0.945
HapMap	African	Sub	120	G=0.017	C=0.983
HapMap	American	Sub	120	G=0.083	C=0.917
HapMap	Asian	Sub	90	G=0.07	C=0.93
Qatari	Global	Study-wide	216	G=0.079	C=0.921
Siberian	Global	Study-wide	54	G=0.04	C=0.96
The Danish reference pan genome	Danish	Study-wide	40	G=0.10	C=0.90

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 12	NC_000012.12:g.11789499G>C
GRCh37.p13 chr 12	NC_000012.11:g.11942433G>C
ETV6 RefSeqGene (LRG_609)	NG_011443.1:g.144646G>C

Gene: ETV6, ETS variant transcription factor 6 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ETV6 transcript variant 1	NM_001987.5:c.163+36920G>C	N/A	Intron Variant
ETV6 transcript variant X1	XM_011520607.3:c.160+3692… XM_011520607.3:c.160+36920G>C	N/A	Intron Variant
ETV6 transcript variant X7	XM_011520611.3:c.-101-496… XM_011520611.3:c.-101-49641G>C	N/A	Intron Variant
ETV6 transcript variant X2	XM_017018990.2:c.163+3692… XM_017018990.2:c.163+36920G>C	N/A	Intron Variant
ETV6 transcript variant X3	XM_017018991.2:c.-1497-36… XM_017018991.2:c.-1497-36145G>C	N/A	Intron Variant
ETV6 transcript variant X1	XM_047428502.1:c.136+3692… XM_047428502.1:c.136+36920G>C	N/A	Intron Variant
ETV6 transcript variant X4	XM_047428503.1:c.-1427-36… XM_047428503.1:c.-1427-36903G>C	N/A	Intron Variant
ETV6 transcript variant X5	XM_047428504.1:c.-1422-36… XM_047428504.1:c.-1422-36908G>C	N/A	Intron Variant
ETV6 transcript variant X6	XM_011520612.3:c.	N/A	Genic Upstream Transcript 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	G=	C
GRCh38.p14 chr 12	NC_000012.12:g.11789499=	NC_000012.12:g.11789499G>C
GRCh37.p13 chr 12	NC_000012.11:g.11942433=	NC_000012.11:g.11942433G>C
ETV6 RefSeqGene (LRG_609)	NG_011443.1:g.144646=	NG_011443.1:g.144646G>C
ETV6 transcript	NM_001987.4:c.163+36920=	NM_001987.4:c.163+36920G>C
ETV6 transcript variant 1	NM_001987.5:c.163+36920=	NM_001987.5:c.163+36920G>C
ETV6 transcript variant X1	XM_011520607.3:c.160+36920=	XM_011520607.3:c.160+36920G>C
ETV6 transcript variant X7	XM_011520611.3:c.-101-49641=	XM_011520611.3:c.-101-49641G>C
ETV6 transcript variant X2	XM_017018990.2:c.163+36920=	XM_017018990.2:c.163+36920G>C
ETV6 transcript variant X3	XM_017018991.2:c.-1497-36145=	XM_017018991.2:c.-1497-36145G>C
ETV6 transcript variant X1	XM_047428502.1:c.136+36920=	XM_047428502.1:c.136+36920G>C
ETV6 transcript variant X4	XM_047428503.1:c.-1427-36903=	XM_047428503.1:c.-1427-36903G>C
ETV6 transcript variant X5	XM_047428504.1:c.-1422-36908=	XM_047428504.1:c.-1422-36908G>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#.

85 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SC_SNP	ss16009972	Feb 27, 2004 (120)
2	SC_SNP	ss18993094	Feb 27, 2004 (120)
3	CSHL-HAPMAP	ss19251157	Feb 27, 2004 (120)
4	SSAHASNP	ss20863426	Apr 05, 2004 (121)
5	PERLEGEN	ss24702365	Sep 20, 2004 (123)
6	ABI	ss40148889	Mar 15, 2006 (126)
7	PERLEGEN	ss69100883	May 18, 2007 (127)
8	HGSV	ss77163975	Dec 07, 2007 (129)
9	BCMHGSC_JDW	ss88972930	Mar 24, 2008 (129)
10	HUMANGENOME_JCVI	ss97207061	Feb 05, 2009 (130)
11	BGI	ss106787719	Feb 05, 2009 (130)
12	1000GENOMES	ss111497208	Jan 25, 2009 (130)
13	1000GENOMES	ss113177939	Jan 25, 2009 (130)
14	ILLUMINA-UK	ss118575811	Feb 14, 2009 (130)
15	ENSEMBL	ss133006604	Dec 01, 2009 (131)
16	ENSEMBL	ss137562774	Dec 01, 2009 (131)
17	GMI	ss157121888	Dec 01, 2009 (131)
18	COMPLETE_GENOMICS	ss167805158	Jul 04, 2010 (132)
19	COMPLETE_GENOMICS	ss169086854	Jul 04, 2010 (132)
20	COMPLETE_GENOMICS	ss170420574	Jul 04, 2010 (132)
21	BUSHMAN	ss203555498	Jul 04, 2010 (132)
22	BCM-HGSC-SUB	ss208105372	Jul 04, 2010 (132)
23	1000GENOMES	ss225609517	Jul 14, 2010 (132)
24	1000GENOMES	ss235826687	Jul 15, 2010 (132)
25	1000GENOMES	ss242405285	Jul 15, 2010 (132)
26	BL	ss254887102	May 09, 2011 (134)
27	GMI	ss281277836	May 04, 2012 (137)
28	GMI	ss286507691	Apr 25, 2013 (138)
29	PJP	ss291381698	May 09, 2011 (134)
30	TISHKOFF	ss562996325	Apr 25, 2013 (138)
31	EVA-GONL	ss989244084	Aug 21, 2014 (142)
32	JMKIDD_LAB	ss1078250733	Aug 21, 2014 (142)
33	1000GENOMES	ss1343934560	Aug 21, 2014 (142)
34	HAMMER_LAB	ss1397625817	Sep 08, 2015 (146)
35	DDI	ss1426846514	Apr 01, 2015 (144)
36	EVA_GENOME_DK	ss1576116833	Apr 01, 2015 (144)
37	EVA_DECODE	ss1598913300	Apr 01, 2015 (144)
38	EVA_UK10K_ALSPAC	ss1628023370	Apr 01, 2015 (144)
39	EVA_UK10K_TWINSUK	ss1671017403	Apr 01, 2015 (144)
40	HAMMER_LAB	ss1807122903	Sep 08, 2015 (146)
41	WEILL_CORNELL_DGM	ss1932609982	Feb 12, 2016 (147)
42	ILLUMINA	ss1959414165	Feb 12, 2016 (147)
43	GENOMED	ss1967524707	Jul 19, 2016 (147)
44	JJLAB	ss2027049623	Sep 14, 2016 (149)
45	USC_VALOUEV	ss2155374125	Dec 20, 2016 (150)
46	HUMAN_LONGEVITY	ss2187808171	Dec 20, 2016 (150)
47	SYSTEMSBIOZJU	ss2628004120	Nov 08, 2017 (151)
48	GRF	ss2699699591	Nov 08, 2017 (151)
49	GNOMAD	ss2907407324	Nov 08, 2017 (151)
50	AFFY	ss2984968214	Nov 08, 2017 (151)
51	SWEGEN	ss3009218969	Nov 08, 2017 (151)
52	ILLUMINA	ss3021406909	Nov 08, 2017 (151)
53	BIOINF_KMB_FNS_UNIBA	ss3027330021	Nov 08, 2017 (151)
54	CSHL	ss3349927351	Nov 08, 2017 (151)
55	URBANLAB	ss3649769496	Oct 12, 2018 (152)
56	ILLUMINA	ss3651780331	Oct 12, 2018 (152)
57	EGCUT_WGS	ss3676530757	Jul 13, 2019 (153)
58	EVA_DECODE	ss3693124034	Jul 13, 2019 (153)
59	ILLUMINA	ss3725303666	Jul 13, 2019 (153)
60	ACPOP	ss3738775496	Jul 13, 2019 (153)
61	EVA	ss3750147212	Jul 13, 2019 (153)
62	PAGE_CC	ss3771674857	Jul 13, 2019 (153)
63	PACBIO	ss3787145449	Jul 13, 2019 (153)
64	PACBIO	ss3792259104	Jul 13, 2019 (153)
65	PACBIO	ss3797141688	Jul 13, 2019 (153)
66	KHV_HUMAN_GENOMES	ss3815463892	Jul 13, 2019 (153)
67	EVA	ss3832978122	Apr 26, 2020 (154)
68	EVA	ss3840054676	Apr 26, 2020 (154)
69	EVA	ss3845538035	Apr 26, 2020 (154)
70	SGDP_PRJ	ss3877703626	Apr 26, 2020 (154)
71	KRGDB	ss3926219804	Apr 26, 2020 (154)
72	TOPMED	ss4908826817	Apr 26, 2021 (155)
73	TOMMO_GENOMICS	ss5205088835	Apr 26, 2021 (155)
74	1000G_HIGH_COVERAGE	ss5289826270	Oct 16, 2022 (156)
75	EVA	ss5403949691	Oct 16, 2022 (156)
76	HUGCELL_USP	ss5484707644	Oct 16, 2022 (156)
77	1000G_HIGH_COVERAGE	ss5586759657	Oct 16, 2022 (156)
78	SANFORD_IMAGENETICS	ss5652604244	Oct 16, 2022 (156)
79	TOMMO_GENOMICS	ss5753897439	Oct 16, 2022 (156)
80	YY_MCH	ss5813018214	Oct 16, 2022 (156)
81	EVA	ss5837596956	Oct 16, 2022 (156)
82	EVA	ss5850262494	Oct 16, 2022 (156)
83	EVA	ss5903301565	Oct 16, 2022 (156)
84	EVA	ss5943949952	Oct 16, 2022 (156)
85	EVA	ss5980722515	Oct 16, 2022 (156)
86	1000Genomes	NC_000012.11 - 11942433	Oct 12, 2018 (152)
87	1000Genomes_30x	NC_000012.12 - 11789499	Oct 16, 2022 (156)
88	The Avon Longitudinal Study of Parents and Children	NC_000012.11 - 11942433	Oct 12, 2018 (152)
89	Genome-wide autozygosity in Daghestan	NC_000012.10 - 11833700	Apr 26, 2020 (154)
90	Genetic variation in the Estonian population	NC_000012.11 - 11942433	Oct 12, 2018 (152)
91	The Danish reference pan genome	NC_000012.11 - 11942433	Apr 26, 2020 (154)
92	gnomAD - Genomes	NC_000012.12 - 11789499	Apr 26, 2021 (155)
93	Genome of the Netherlands Release 5	NC_000012.11 - 11942433	Apr 26, 2020 (154)
94	HapMap	NC_000012.12 - 11789499	Apr 26, 2020 (154)
95	KOREAN population from KRGDB	NC_000012.11 - 11942433	Apr 26, 2020 (154)
96	Northern Sweden	NC_000012.11 - 11942433	Jul 13, 2019 (153)
97	The PAGE Study	NC_000012.12 - 11789499	Jul 13, 2019 (153)
98	Qatari	NC_000012.11 - 11942433	Apr 26, 2020 (154)
99	SGDP_PRJ	NC_000012.11 - 11942433	Apr 26, 2020 (154)
100	Siberian	NC_000012.11 - 11942433	Apr 26, 2020 (154)
101	8.3KJPN	NC_000012.11 - 11942433	Apr 26, 2021 (155)
102	14KJPN	NC_000012.12 - 11789499	Oct 16, 2022 (156)
103	TopMed	NC_000012.12 - 11789499	Apr 26, 2021 (155)
104	UK 10K study - Twins	NC_000012.11 - 11942433	Oct 12, 2018 (152)
105	ALFA	NC_000012.12 - 11789499	Apr 26, 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)
rs17746206	Oct 08, 2004 (123)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss77163975	NC_000012.9:11833699:G:C	NC_000012.12:11789498:G:C	(self)
96818, ss88972930, ss111497208, ss113177939, ss118575811, ss167805158, ss169086854, ss170420574, ss203555498, ss208105372, ss254887102, ss281277836, ss286507691, ss291381698, ss1397625817, ss1598913300	NC_000012.10:11833699:G:C	NC_000012.12:11789498:G:C	(self)
56642904, 31449144, 22269005, 2845941, 14032189, 33397198, 12060361, 14651912, 29720606, 7890479, 63058142, 31449144, ss225609517, ss235826687, ss242405285, ss562996325, ss989244084, ss1078250733, ss1343934560, ss1426846514, ss1576116833, ss1628023370, ss1671017403, ss1807122903, ss1932609982, ss1959414165, ss1967524707, ss2027049623, ss2155374125, ss2628004120, ss2699699591, ss2907407324, ss2984968214, ss3009218969, ss3021406909, ss3349927351, ss3651780331, ss3676530757, ss3738775496, ss3750147212, ss3787145449, ss3792259104, ss3797141688, ss3832978122, ss3840054676, ss3877703626, ss3926219804, ss5205088835, ss5403949691, ss5652604244, ss5837596956, ss5943949952, ss5980722515	NC_000012.11:11942432:G:C	NC_000012.12:11789498:G:C	(self)
74285592, 399402698, 756379, 896326, 87734543, 124372474, 11067640083, ss2187808171, ss3027330021, ss3649769496, ss3693124034, ss3725303666, ss3771674857, ss3815463892, ss3845538035, ss4908826817, ss5289826270, ss5484707644, ss5586759657, ss5753897439, ss5813018214, ss5850262494, ss5903301565	NC_000012.12:11789498:G:C	NC_000012.12:11789498:G:C	(self)
ss16009972, ss18993094, ss19251157, ss20863426	NT_009714.16:4701406:G:C	NC_000012.12:11789498:G:C	(self)
ss24702365, ss40148889, ss69100883, ss97207061, ss106787719, ss133006604, ss137562774, ss157121888	NT_009714.17:4702556:G:C	NC_000012.12:11789498:G: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 rs10845411

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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs10845411