Name: rs10278483
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.

rs10278483

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:87702649 (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 / T>G
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.031252 (4784/153080, ALFA)
C=0.11069 (3128/28258, 14KJPN)
C=0.10866 (1821/16758, 8.3KJPN) (+ 15 more)
C=0.0670 (429/6404, 1000G_30x)
C=0.0653 (327/5008, 1000G)
C=0.0283 (127/4480, Estonian)
C=0.0259 (100/3854, ALSPAC)
C=0.0245 (91/3708, TWINSUK)
C=0.1259 (369/2930, KOREAN)
C=0.0666 (126/1892, HapMap)
C=0.1201 (220/1832, Korea1K)
C=0.019 (19/998, GoNL)
C=0.075 (47/626, Chileans)
C=0.022 (13/600, NorthernSweden)
C=0.014 (3/216, Qatari)
C=0.051 (11/214, Vietnamese)
T=0.47 (34/72, SGDP_PRJ)
C=0.05 (2/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ABCB1 : Intron Variant
RUNDC3B : 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	153080	T=0.968748	C=0.031252, G=0.000000
European	Sub	129278	T=0.973453	C=0.026547, G=0.000000
African	Sub	6844	T=0.9487	C=0.0513, G=0.0000
African Others	Sub	232	T=0.935	C=0.065, G=0.000
African American	Sub	6612	T=0.9492	C=0.0508, G=0.0000
Asian	Sub	656	T=0.910	C=0.090, G=0.000
East Asian	Sub	494	T=0.917	C=0.083, G=0.000
Other Asian	Sub	162	T=0.889	C=0.111, G=0.000
Latin American 1	Sub	876	T=0.966	C=0.034, G=0.000
Latin American 2	Sub	8386	T=0.9277	C=0.0723, G=0.0000
South Asian	Sub	190	T=0.989	C=0.011, G=0.000
Other	Sub	6850	T=0.9556	C=0.0444, G=0.0000

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
Allele Frequency Aggregator	Total	Global	153080	T=0.968748	C=0.031252, G=0.000000
Allele Frequency Aggregator	European	Sub	129278	T=0.973453	C=0.026547, G=0.000000
Allele Frequency Aggregator	Latin American 2	Sub	8386	T=0.9277	C=0.0723, G=0.0000
Allele Frequency Aggregator	Other	Sub	6850	T=0.9556	C=0.0444, G=0.0000
Allele Frequency Aggregator	African	Sub	6844	T=0.9487	C=0.0513, G=0.0000
Allele Frequency Aggregator	Latin American 1	Sub	876	T=0.966	C=0.034, G=0.000
Allele Frequency Aggregator	Asian	Sub	656	T=0.910	C=0.090, G=0.000
Allele Frequency Aggregator	South Asian	Sub	190	T=0.989	C=0.011, G=0.000
14KJPN	JAPANESE	Study-wide	28258	T=0.88931	C=0.11069
8.3KJPN	JAPANESE	Study-wide	16758	T=0.89134	C=0.10866
1000Genomes_30x	Global	Study-wide	6404	T=0.9330	C=0.0670
1000Genomes_30x	African	Sub	1786	T=0.9009	C=0.0991
1000Genomes_30x	Europe	Sub	1266	T=0.9763	C=0.0237
1000Genomes_30x	South Asian	Sub	1202	T=0.9609	C=0.0391
1000Genomes_30x	East Asian	Sub	1170	T=0.9179	C=0.0821
1000Genomes_30x	American	Sub	980	T=0.919	C=0.081
1000Genomes	Global	Study-wide	5008	T=0.9347	C=0.0653
1000Genomes	African	Sub	1322	T=0.9009	C=0.0991
1000Genomes	East Asian	Sub	1008	T=0.9147	C=0.0853
1000Genomes	Europe	Sub	1006	T=0.9771	C=0.0229
1000Genomes	South Asian	Sub	978	T=0.965	C=0.035
1000Genomes	American	Sub	694	T=0.924	C=0.076
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.9717	C=0.0283
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.9741	C=0.0259
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.9755	C=0.0245
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.8741	C=0.1259
HapMap	Global	Study-wide	1892	T=0.9334	C=0.0666
HapMap	American	Sub	770	T=0.948	C=0.052
HapMap	African	Sub	692	T=0.923	C=0.077
HapMap	Asian	Sub	254	T=0.906	C=0.094
HapMap	Europe	Sub	176	T=0.949	C=0.051
Korean Genome Project	KOREAN	Study-wide	1832	T=0.8799	C=0.1201
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.981	C=0.019
Chileans	Chilean	Study-wide	626	T=0.925	C=0.075
Northern Sweden	ACPOP	Study-wide	600	T=0.978	C=0.022
Qatari	Global	Study-wide	216	T=0.986	C=0.014
A Vietnamese Genetic Variation Database	Global	Study-wide	214	T=0.949	C=0.051
SGDP_PRJ	Global	Study-wide	72	T=0.47	C=0.53
The Danish reference pan genome	Danish	Study-wide	40	T=0.95	C=0.05

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 7	NC_000007.14:g.87702649T>C
GRCh38.p14 chr 7	NC_000007.14:g.87702649T>G
GRCh37.p13 chr 7	NC_000007.13:g.87331965T>C
GRCh37.p13 chr 7	NC_000007.13:g.87331965T>G
ABCB1 RefSeqGene	NG_011513.1:g.15600A>G
ABCB1 RefSeqGene	NG_011513.1:g.15600A>C

Gene: ABCB1, ATP binding cassette subfamily B member 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ABCB1 transcript variant 3	NM_000927.5:c.-331+10512A… NM_000927.5:c.-331+10512A>G	N/A	Intron Variant
ABCB1 transcript variant 2	NM_001348944.2:c.-184+105… NM_001348944.2:c.-184+10512A>G	N/A	Intron Variant
ABCB1 transcript variant 1	NM_001348945.2:c.-172-991… NM_001348945.2:c.-172-991A>G	N/A	Intron Variant
ABCB1 transcript variant 4	NM_001348946.2:c.	N/A	Genic Upstream Transcript Variant

Gene: RUNDC3B, RUN domain containing 3B (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
RUNDC3B transcript variant 2	NM_001134405.2:c.372+2095… NM_001134405.2:c.372+2095T>C	N/A	Intron Variant
RUNDC3B transcript variant 3	NM_001134406.2:c.372+2095… NM_001134406.2:c.372+2095T>C	N/A	Intron Variant
RUNDC3B transcript variant 4	NM_001394224.1:c.423+2095… NM_001394224.1:c.423+2095T>C	N/A	Intron Variant
RUNDC3B transcript variant 5	NM_001394225.1:c.372+2095… NM_001394225.1:c.372+2095T>C	N/A	Intron Variant
RUNDC3B transcript variant 6	NM_001394226.1:c.372+2095… NM_001394226.1:c.372+2095T>C	N/A	Intron Variant
RUNDC3B transcript variant 7	NM_001394227.1:c.423+2095… NM_001394227.1:c.423+2095T>C	N/A	Intron Variant
RUNDC3B transcript variant 8	NM_001394228.1:c.30+2095T… NM_001394228.1:c.30+2095T>C	N/A	Intron Variant
RUNDC3B transcript variant 1	NM_138290.3:c.423+2095T>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.

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	G
GRCh38.p14 chr 7	NC_000007.14:g.87702649=	NC_000007.14:g.87702649T>C	NC_000007.14:g.87702649T>G
GRCh37.p13 chr 7	NC_000007.13:g.87331965=	NC_000007.13:g.87331965T>C	NC_000007.13:g.87331965T>G
ABCB1 RefSeqGene	NG_011513.1:g.15600=	NG_011513.1:g.15600A>G	NG_011513.1:g.15600A>C
ABCB1 transcript variant 3	NM_000927.4:c.-331+10512=	NM_000927.4:c.-331+10512A>G	NM_000927.4:c.-331+10512A>C
ABCB1 transcript variant 3	NM_000927.5:c.-331+10512=	NM_000927.5:c.-331+10512A>G	NM_000927.5:c.-331+10512A>C
RUNDC3B transcript variant 2	NM_001134405.1:c.372+2095=	NM_001134405.1:c.372+2095T>C	NM_001134405.1:c.372+2095T>G
RUNDC3B transcript variant 2	NM_001134405.2:c.372+2095=	NM_001134405.2:c.372+2095T>C	NM_001134405.2:c.372+2095T>G
RUNDC3B transcript variant 3	NM_001134406.1:c.372+2095=	NM_001134406.1:c.372+2095T>C	NM_001134406.1:c.372+2095T>G
RUNDC3B transcript variant 3	NM_001134406.2:c.372+2095=	NM_001134406.2:c.372+2095T>C	NM_001134406.2:c.372+2095T>G
ABCB1 transcript variant 2	NM_001348944.2:c.-184+10512=	NM_001348944.2:c.-184+10512A>G	NM_001348944.2:c.-184+10512A>C
ABCB1 transcript variant 1	NM_001348945.2:c.-172-991=	NM_001348945.2:c.-172-991A>G	NM_001348945.2:c.-172-991A>C
RUNDC3B transcript variant 4	NM_001394224.1:c.423+2095=	NM_001394224.1:c.423+2095T>C	NM_001394224.1:c.423+2095T>G
RUNDC3B transcript variant 5	NM_001394225.1:c.372+2095=	NM_001394225.1:c.372+2095T>C	NM_001394225.1:c.372+2095T>G
RUNDC3B transcript variant 6	NM_001394226.1:c.372+2095=	NM_001394226.1:c.372+2095T>C	NM_001394226.1:c.372+2095T>G
RUNDC3B transcript variant 7	NM_001394227.1:c.423+2095=	NM_001394227.1:c.423+2095T>C	NM_001394227.1:c.423+2095T>G
RUNDC3B transcript variant 8	NM_001394228.1:c.30+2095=	NM_001394228.1:c.30+2095T>C	NM_001394228.1:c.30+2095T>G
RUNDC3B transcript variant 1	NM_138290.2:c.423+2095=	NM_138290.2:c.423+2095T>C	NM_138290.2:c.423+2095T>G
RUNDC3B transcript variant 1	NM_138290.3:c.423+2095=	NM_138290.3:c.423+2095T>C	NM_138290.3:c.423+2095T>G
RUNDC3B transcript variant X1	XM_005250156.1:c.372+2095=	XM_005250156.1:c.372+2095T>C	XM_005250156.1:c.372+2095T>G
RUNDC3B transcript variant X2	XM_005250157.1:c.30+2095=	XM_005250157.1:c.30+2095T>C	XM_005250157.1:c.30+2095T>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#.

76 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	WUGSC_SSAHASNP	ss14148323	Dec 05, 2003 (119)
2	ILLUMINA	ss75255253	Dec 06, 2007 (129)
3	AFFY	ss76449461	Dec 08, 2007 (130)
4	KRIBB_YJKIM	ss80781893	Dec 14, 2007 (130)
5	KRIBB_YJKIM	ss119619968	Dec 01, 2009 (131)
6	ILLUMINA	ss159886274	Dec 01, 2009 (131)
7	ILLUMINA	ss169975250	Jul 04, 2010 (132)
8	1000GENOMES	ss223188424	Jul 14, 2010 (132)
9	1000GENOMES	ss234064295	Jul 15, 2010 (132)
10	1000GENOMES	ss241002228	Jul 15, 2010 (132)
11	GMI	ss279426305	May 04, 2012 (137)
12	ILLUMINA	ss479247204	May 04, 2012 (137)
13	ILLUMINA	ss479249945	May 04, 2012 (137)
14	ILLUMINA	ss479611001	Sep 08, 2015 (146)
15	ILLUMINA	ss484424311	May 04, 2012 (137)
16	ILLUMINA	ss536598240	Sep 08, 2015 (146)
17	SSMP	ss654534460	Apr 25, 2013 (138)
18	ILLUMINA	ss778353841	Sep 08, 2015 (146)
19	ILLUMINA	ss782658611	Sep 08, 2015 (146)
20	ILLUMINA	ss783627688	Sep 08, 2015 (146)
21	ILLUMINA	ss831909074	Sep 08, 2015 (146)
22	ILLUMINA	ss833808557	Sep 08, 2015 (146)
23	EVA-GONL	ss984508099	Aug 21, 2014 (142)
24	JMKIDD_LAB	ss1074772300	Aug 21, 2014 (142)
25	1000GENOMES	ss1326018897	Aug 21, 2014 (142)
26	EVA_GENOME_DK	ss1582294488	Apr 01, 2015 (144)
27	EVA_DECODE	ss1594084011	Apr 01, 2015 (144)
28	EVA_UK10K_ALSPAC	ss1618633037	Apr 01, 2015 (144)
29	EVA_UK10K_TWINSUK	ss1661627070	Apr 01, 2015 (144)
30	EVA_SVP	ss1712968924	Apr 01, 2015 (144)
31	ILLUMINA	ss1752698359	Sep 08, 2015 (146)
32	WEILL_CORNELL_DGM	ss1927771211	Feb 12, 2016 (147)
33	GENOMED	ss1970753260	Jul 19, 2016 (147)
34	JJLAB	ss2024567952	Sep 14, 2016 (149)
35	HUMAN_LONGEVITY	ss2295541587	Dec 20, 2016 (150)
36	ILLUMINA	ss2634629146	Nov 08, 2017 (151)
37	GRF	ss2708493446	Nov 08, 2017 (151)
38	GNOMAD	ss2855829302	Nov 08, 2017 (151)
39	SWEGEN	ss3001579336	Nov 08, 2017 (151)
40	ILLUMINA	ss3629856814	Oct 12, 2018 (152)
41	ILLUMINA	ss3632535314	Oct 12, 2018 (152)
42	ILLUMINA	ss3633469432	Oct 12, 2018 (152)
43	ILLUMINA	ss3634194671	Oct 12, 2018 (152)
44	ILLUMINA	ss3635129191	Oct 12, 2018 (152)
45	ILLUMINA	ss3635874320	Oct 12, 2018 (152)
46	ILLUMINA	ss3636862657	Oct 12, 2018 (152)
47	ILLUMINA	ss3637627321	Oct 12, 2018 (152)
48	ILLUMINA	ss3638708449	Oct 12, 2018 (152)
49	ILLUMINA	ss3640836483	Oct 12, 2018 (152)
50	ILLUMINA	ss3643643531	Oct 12, 2018 (152)
51	EGCUT_WGS	ss3669332976	Jul 13, 2019 (153)
52	EVA_DECODE	ss3720148306	Jul 13, 2019 (153)
53	ACPOP	ss3734835262	Jul 13, 2019 (153)
54	ILLUMINA	ss3745429208	Jul 13, 2019 (153)
55	EVA	ss3766829872	Jul 13, 2019 (153)
56	ILLUMINA	ss3772922111	Jul 13, 2019 (153)
57	KHV_HUMAN_GENOMES	ss3810003328	Jul 13, 2019 (153)
58	SGDP_PRJ	ss3867818539	Apr 26, 2020 (154)
59	KRGDB	ss3915079638	Apr 26, 2020 (154)
60	KOGIC	ss3962030609	Apr 26, 2020 (154)
61	TOPMED	ss4753680341	Apr 26, 2021 (155)
62	TOPMED	ss4753680342	Apr 26, 2021 (155)
63	TOMMO_GENOMICS	ss5184292584	Apr 26, 2021 (155)
64	1000G_HIGH_COVERAGE	ss5273750901	Oct 16, 2022 (156)
65	EVA	ss5315261599	Oct 16, 2022 (156)
66	EVA	ss5374988326	Oct 16, 2022 (156)
67	HUGCELL_USP	ss5470749817	Oct 16, 2022 (156)
68	EVA	ss5509036903	Oct 16, 2022 (156)
69	1000G_HIGH_COVERAGE	ss5562383791	Oct 16, 2022 (156)
70	SANFORD_IMAGENETICS	ss5643430641	Oct 16, 2022 (156)
71	TOMMO_GENOMICS	ss5724892147	Oct 16, 2022 (156)
72	EVA	ss5799729911	Oct 16, 2022 (156)
73	YY_MCH	ss5808857536	Oct 16, 2022 (156)
74	EVA	ss5823149217	Oct 16, 2022 (156)
75	EVA	ss5859767934	Oct 16, 2022 (156)
76	EVA	ss5972607571	Oct 16, 2022 (156)
77	1000Genomes	NC_000007.13 - 87331965	Oct 12, 2018 (152)
78	1000Genomes_30x	NC_000007.14 - 87702649	Oct 16, 2022 (156)
79	The Avon Longitudinal Study of Parents and Children	NC_000007.13 - 87331965	Oct 12, 2018 (152)
80	Chileans	NC_000007.13 - 87331965	Apr 26, 2020 (154)
81	Genetic variation in the Estonian population	NC_000007.13 - 87331965	Oct 12, 2018 (152)
82	The Danish reference pan genome	NC_000007.13 - 87331965	Apr 26, 2020 (154)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 268239948 (NC_000007.14:87702648:T:C 6995/140148) Row 268239949 (NC_000007.14:87702648:T:G 2/140172)	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 268239948 (NC_000007.14:87702648:T:C 6995/140148) Row 268239949 (NC_000007.14:87702648:T:G 2/140172)	-	Apr 26, 2021 (155)
85	Genome of the Netherlands Release 5	NC_000007.13 - 87331965	Apr 26, 2020 (154)
86	HapMap	NC_000007.14 - 87702649	Apr 26, 2020 (154)
87	KOREAN population from KRGDB	NC_000007.13 - 87331965	Apr 26, 2020 (154)
88	Korean Genome Project	NC_000007.14 - 87702649	Apr 26, 2020 (154)
89	Northern Sweden	NC_000007.13 - 87331965	Jul 13, 2019 (153)
90	Qatari	NC_000007.13 - 87331965	Apr 26, 2020 (154)
91	SGDP_PRJ	NC_000007.13 - 87331965	Apr 26, 2020 (154)
92	8.3KJPN	NC_000007.13 - 87331965	Apr 26, 2021 (155)
93	14KJPN	NC_000007.14 - 87702649	Oct 16, 2022 (156)
94	TopMed Submission ignored due to conflicting rows: Row 591057900 (NC_000007.14:87702648:T:C 14592/264690) Row 591057901 (NC_000007.14:87702648:T:G 3/264690)	-	Apr 26, 2021 (155)
95	TopMed Submission ignored due to conflicting rows: Row 591057900 (NC_000007.14:87702648:T:C 14592/264690) Row 591057901 (NC_000007.14:87702648:T:G 3/264690)	-	Apr 26, 2021 (155)
96	UK 10K study - Twins	NC_000007.13 - 87331965	Oct 12, 2018 (152)
97	A Vietnamese Genetic Variation Database	NC_000007.13 - 87331965	Jul 13, 2019 (153)
98	ALFA	NC_000007.14 - 87702649	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)
rs56423967	May 24, 2008 (130)
rs58010283	May 24, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss76449461, ss279426305, ss479247204, ss1594084011, ss1712968924, ss3643643531	NC_000007.12:87169900:T:C	NC_000007.14:87702648:T:C	(self)
38021000, 21157362, 413775, 15071224, 8459427, 9447304, 22257032, 8120127, 9813141, 19835519, 42261891, 21157362, 4719137, ss223188424, ss234064295, ss241002228, ss479249945, ss479611001, ss484424311, ss536598240, ss654534460, ss778353841, ss782658611, ss783627688, ss831909074, ss833808557, ss984508099, ss1074772300, ss1326018897, ss1582294488, ss1618633037, ss1661627070, ss1752698359, ss1927771211, ss1970753260, ss2024567952, ss2634629146, ss2708493446, ss2855829302, ss3001579336, ss3629856814, ss3632535314, ss3633469432, ss3634194671, ss3635129191, ss3635874320, ss3636862657, ss3637627321, ss3638708449, ss3640836483, ss3669332976, ss3734835262, ss3745429208, ss3766829872, ss3772922111, ss3867818539, ss3915079638, ss5184292584, ss5315261599, ss5374988326, ss5509036903, ss5643430641, ss5799729911, ss5823149217, ss5972607571	NC_000007.13:87331964:T:C	NC_000007.14:87702648:T:C	(self)
49909726, 3438726, 18408610, 58729251, 6862152796, ss2295541587, ss3720148306, ss3810003328, ss3962030609, ss4753680341, ss5273750901, ss5470749817, ss5562383791, ss5724892147, ss5808857536, ss5859767934	NC_000007.14:87702648:T:C	NC_000007.14:87702648:T:C	(self)
ss14148323	NT_007933.13:12566180:T:C	NC_000007.14:87702648:T:C	(self)
ss75255253, ss80781893, ss119619968, ss159886274, ss169975250	NT_007933.15:25364807:T:C	NC_000007.14:87702648:T:C	(self)
ss2855829302	NC_000007.13:87331964:T:G	NC_000007.14:87702648:T:G	(self)
6862152796, ss4753680342	NC_000007.14:87702648:T:G	NC_000007.14:87702648:T: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 rs10278483

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

rs10278483