Name: rs1422978
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.

rs1422978

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr5:170726385 (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>A / T>C / T>G
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.245744 (65046/264690, TOPMED)
T=0.248586 (34809/140028, GnomAD)
T=0.18044 (5099/28258, 14KJPN) (+ 17 more)
T=0.25270 (4494/17784, ALFA)
T=0.18186 (3048/16760, 8.3KJPN)
T=0.2286 (1464/6404, 1000G_30x)
T=0.2306 (1155/5008, 1000G)
T=0.2194 (983/4480, Estonian)
T=0.2745 (1058/3854, ALSPAC)
T=0.2546 (944/3708, TWINSUK)
T=0.1041 (305/2930, KOREAN)
T=0.1032 (189/1832, Korea1K)
T=0.253 (252/998, GoNL)
T=0.238 (143/600, NorthernSweden)
T=0.201 (108/536, SGDP_PRJ)
T=0.182 (60/330, HapMap)
T=0.361 (78/216, Qatari)
T=0.138 (29/210, Vietnamese)
T=0.20 (10/50, Siberian)
T=0.25 (10/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: KCNIP1 : 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	17784	T=0.25270	A=0.00000, C=0.74730
European	Sub	13664	T=0.25315	A=0.00000, C=0.74685
African	Sub	2466	T=0.2717	A=0.0000, C=0.7283
African Others	Sub	98	T=0.27	A=0.00, C=0.73
African American	Sub	2368	T=0.2720	A=0.0000, C=0.7280
Asian	Sub	112	T=0.179	A=0.000, C=0.821
East Asian	Sub	86	T=0.19	A=0.00, C=0.81
Other Asian	Sub	26	T=0.15	A=0.00, C=0.85
Latin American 1	Sub	146	T=0.349	A=0.000, C=0.651
Latin American 2	Sub	610	T=0.167	A=0.000, C=0.833
South Asian	Sub	98	T=0.39	A=0.00, C=0.61
Other	Sub	688	T=0.224	A=0.000, C=0.776

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=0.245744	C=0.754256
gnomAD - Genomes	Global	Study-wide	140028	T=0.248586	C=0.751414
gnomAD - Genomes	European	Sub	75854	T=0.25593	C=0.74407
gnomAD - Genomes	African	Sub	41940	T=0.25806	C=0.74194
gnomAD - Genomes	American	Sub	13636	T=0.19573	C=0.80427
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	T=0.2905	C=0.7095
gnomAD - Genomes	East Asian	Sub	3130	T=0.1319	C=0.8681
gnomAD - Genomes	Other	Sub	2146	T=0.2451	C=0.7549
14KJPN	JAPANESE	Study-wide	28258	T=0.18044	C=0.81956
Allele Frequency Aggregator	Total	Global	17784	T=0.25270	A=0.00000, C=0.74730
Allele Frequency Aggregator	European	Sub	13664	T=0.25315	A=0.00000, C=0.74685
Allele Frequency Aggregator	African	Sub	2466	T=0.2717	A=0.0000, C=0.7283
Allele Frequency Aggregator	Other	Sub	688	T=0.224	A=0.000, C=0.776
Allele Frequency Aggregator	Latin American 2	Sub	610	T=0.167	A=0.000, C=0.833
Allele Frequency Aggregator	Latin American 1	Sub	146	T=0.349	A=0.000, C=0.651
Allele Frequency Aggregator	Asian	Sub	112	T=0.179	A=0.000, C=0.821
Allele Frequency Aggregator	South Asian	Sub	98	T=0.39	A=0.00, C=0.61
8.3KJPN	JAPANESE	Study-wide	16760	T=0.18186	C=0.81814
1000Genomes_30x	Global	Study-wide	6404	T=0.2286	C=0.7714
1000Genomes_30x	African	Sub	1786	T=0.2391	C=0.7609
1000Genomes_30x	Europe	Sub	1266	T=0.2796	C=0.7204
1000Genomes_30x	South Asian	Sub	1202	T=0.3037	C=0.6963
1000Genomes_30x	East Asian	Sub	1170	T=0.1308	C=0.8692
1000Genomes_30x	American	Sub	980	T=0.168	C=0.832
1000Genomes	Global	Study-wide	5008	T=0.2306	C=0.7694
1000Genomes	African	Sub	1322	T=0.2466	C=0.7534
1000Genomes	East Asian	Sub	1008	T=0.1369	C=0.8631
1000Genomes	Europe	Sub	1006	T=0.2813	C=0.7187
1000Genomes	South Asian	Sub	978	T=0.302	C=0.698
1000Genomes	American	Sub	694	T=0.163	C=0.837
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.2194	C=0.7806
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.2745	C=0.7255
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.2546	C=0.7454
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.1041	A=0.0000, C=0.8959, G=0.0000
Korean Genome Project	KOREAN	Study-wide	1832	T=0.1032	C=0.8968
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.253	C=0.747
Northern Sweden	ACPOP	Study-wide	600	T=0.238	C=0.762
SGDP_PRJ	Global	Study-wide	536	T=0.201	C=0.799
HapMap	Global	Study-wide	330	T=0.182	C=0.818
HapMap	African	Sub	120	T=0.142	C=0.858
HapMap	American	Sub	120	T=0.233	C=0.767
HapMap	Asian	Sub	90	T=0.17	C=0.83
Qatari	Global	Study-wide	216	T=0.361	C=0.639
A Vietnamese Genetic Variation Database	Global	Study-wide	210	T=0.138	C=0.862
Siberian	Global	Study-wide	50	T=0.20	C=0.80
The Danish reference pan genome	Danish	Study-wide	40	T=0.25	C=0.75

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 5	NC_000005.10:g.170726385T>A
GRCh38.p14 chr 5	NC_000005.10:g.170726385T>C
GRCh38.p14 chr 5	NC_000005.10:g.170726385T>G
GRCh37.p13 chr 5	NC_000005.9:g.170153389T>A
GRCh37.p13 chr 5	NC_000005.9:g.170153389T>C
GRCh37.p13 chr 5	NC_000005.9:g.170153389T>G
KCNIP1 RefSeqGene	NG_011538.2:g.377509T>A
KCNIP1 RefSeqGene	NG_011538.2:g.377509T>C
KCNIP1 RefSeqGene	NG_011538.2:g.377509T>G

Gene: KCNIP1, potassium voltage-gated channel interacting protein 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
KCNIP1 transcript variant 1	NM_001034837.3:c.468+3565… NM_001034837.3:c.468+3565T>A	N/A	Intron Variant
KCNIP1 transcript variant 3	NM_001034838.3:c.462+3565… NM_001034838.3:c.462+3565T>A	N/A	Intron Variant
KCNIP1 transcript variant 5	NM_001278339.2:c.510+3565… NM_001278339.2:c.510+3565T>A	N/A	Intron Variant
KCNIP1 transcript variant 4	NM_001278340.2:c.351+3565… NM_001278340.2:c.351+3565T>A	N/A	Intron Variant
KCNIP1 transcript variant 2	NM_014592.4:c.435+3565T>A	N/A	Intron Variant
KCNIP1 transcript variant X1	XM_017009407.2:c.462+3565… XM_017009407.2:c.462+3565T>A	N/A	Intron Variant
KCNIP1 transcript variant X2	XM_017009408.2:c.	N/A	Genic Downstream 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	T=	A	C	G
GRCh38.p14 chr 5	NC_000005.10:g.170726385=	NC_000005.10:g.170726385T>A	NC_000005.10:g.170726385T>C	NC_000005.10:g.170726385T>G
GRCh37.p13 chr 5	NC_000005.9:g.170153389=	NC_000005.9:g.170153389T>A	NC_000005.9:g.170153389T>C	NC_000005.9:g.170153389T>G
KCNIP1 RefSeqGene	NG_011538.2:g.377509=	NG_011538.2:g.377509T>A	NG_011538.2:g.377509T>C	NG_011538.2:g.377509T>G
KCNIP1 transcript variant 1	NM_001034837.2:c.468+3565=	NM_001034837.2:c.468+3565T>A	NM_001034837.2:c.468+3565T>C	NM_001034837.2:c.468+3565T>G
KCNIP1 transcript variant 1	NM_001034837.3:c.468+3565=	NM_001034837.3:c.468+3565T>A	NM_001034837.3:c.468+3565T>C	NM_001034837.3:c.468+3565T>G
KCNIP1 transcript variant 3	NM_001034838.2:c.462+3565=	NM_001034838.2:c.462+3565T>A	NM_001034838.2:c.462+3565T>C	NM_001034838.2:c.462+3565T>G
KCNIP1 transcript variant 3	NM_001034838.3:c.462+3565=	NM_001034838.3:c.462+3565T>A	NM_001034838.3:c.462+3565T>C	NM_001034838.3:c.462+3565T>G
KCNIP1 transcript variant 5	NM_001278339.1:c.510+3565=	NM_001278339.1:c.510+3565T>A	NM_001278339.1:c.510+3565T>C	NM_001278339.1:c.510+3565T>G
KCNIP1 transcript variant 5	NM_001278339.2:c.510+3565=	NM_001278339.2:c.510+3565T>A	NM_001278339.2:c.510+3565T>C	NM_001278339.2:c.510+3565T>G
KCNIP1 transcript variant 4	NM_001278340.1:c.351+3565=	NM_001278340.1:c.351+3565T>A	NM_001278340.1:c.351+3565T>C	NM_001278340.1:c.351+3565T>G
KCNIP1 transcript variant 4	NM_001278340.2:c.351+3565=	NM_001278340.2:c.351+3565T>A	NM_001278340.2:c.351+3565T>C	NM_001278340.2:c.351+3565T>G
KCNIP1 transcript variant 2	NM_014592.3:c.435+3565=	NM_014592.3:c.435+3565T>A	NM_014592.3:c.435+3565T>C	NM_014592.3:c.435+3565T>G
KCNIP1 transcript variant 2	NM_014592.4:c.435+3565=	NM_014592.4:c.435+3565T>A	NM_014592.4:c.435+3565T>C	NM_014592.4:c.435+3565T>G
KCNIP1 transcript variant X1	XM_017009407.2:c.462+3565=	XM_017009407.2:c.462+3565T>A	XM_017009407.2:c.462+3565T>C	XM_017009407.2:c.462+3565T>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#.

77 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss2228495	Oct 23, 2000 (88)
2	WI_SSAHASNP	ss14641829	Dec 05, 2003 (123)
3	SC_SNP	ss14814085	Dec 05, 2003 (119)
4	CSHL-HAPMAP	ss17086438	Feb 27, 2004 (120)
5	ABI	ss42528650	Mar 14, 2006 (126)
6	HGSV	ss83665282	Dec 15, 2007 (130)
7	HGSV	ss83959795	Dec 15, 2007 (130)
8	BCMHGSC_JDW	ss93333694	Mar 24, 2008 (129)
9	BGI	ss105969163	Feb 05, 2009 (130)
10	1000GENOMES	ss109622034	Jan 24, 2009 (130)
11	1000GENOMES	ss113657407	Jan 25, 2009 (130)
12	ILLUMINA-UK	ss116906412	Dec 01, 2009 (131)
13	ENSEMBL	ss143617711	Dec 01, 2009 (131)
14	GMI	ss156333222	Dec 01, 2009 (131)
15	COMPLETE_GENOMICS	ss162887095	Jul 04, 2010 (132)
16	COMPLETE_GENOMICS	ss166228365	Jul 04, 2010 (132)
17	COMPLETE_GENOMICS	ss167363022	Jul 04, 2010 (132)
18	BUSHMAN	ss201203372	Jul 04, 2010 (132)
19	BCM-HGSC-SUB	ss206706825	Jul 04, 2010 (132)
20	1000GENOMES	ss222115457	Jul 14, 2010 (132)
21	1000GENOMES	ss233255751	Jul 14, 2010 (132)
22	1000GENOMES	ss240356424	Jul 15, 2010 (132)
23	BL	ss253946274	May 09, 2011 (134)
24	GMI	ss278585720	May 04, 2012 (137)
25	GMI	ss285308475	Apr 25, 2013 (138)
26	PJP	ss293520240	May 09, 2011 (134)
27	TISHKOFF	ss558887643	Apr 25, 2013 (138)
28	SSMP	ss652797546	Apr 25, 2013 (138)
29	EVA-GONL	ss982409315	Aug 21, 2014 (142)
30	JMKIDD_LAB	ss1073255739	Aug 21, 2014 (142)
31	1000GENOMES	ss1318317689	Aug 21, 2014 (142)
32	DDI	ss1430582415	Apr 01, 2015 (144)
33	EVA_GENOME_DK	ss1581461587	Apr 01, 2015 (144)
34	EVA_DECODE	ss1591951872	Apr 01, 2015 (144)
35	EVA_UK10K_ALSPAC	ss1614606843	Apr 01, 2015 (144)
36	EVA_UK10K_TWINSUK	ss1657600876	Apr 01, 2015 (144)
37	HAMMER_LAB	ss1804199805	Sep 08, 2015 (146)
38	WEILL_CORNELL_DGM	ss1925658885	Feb 12, 2016 (147)
39	GENOMED	ss1970271001	Jul 19, 2016 (147)
40	JJLAB	ss2023443173	Sep 14, 2016 (149)
41	USC_VALOUEV	ss2151602942	Dec 20, 2016 (150)
42	HUMAN_LONGEVITY	ss2280477446	Dec 20, 2016 (150)
43	SYSTEMSBIOZJU	ss2626209758	Nov 08, 2017 (151)
44	GRF	ss2707179326	Nov 08, 2017 (151)
45	GNOMAD	ss2833922658	Nov 08, 2017 (151)
46	SWEGEN	ss2998233502	Nov 08, 2017 (151)
47	BIOINF_KMB_FNS_UNIBA	ss3025504502	Nov 08, 2017 (151)
48	CSHL	ss3346750929	Nov 08, 2017 (151)
49	URBANLAB	ss3648227204	Oct 12, 2018 (152)
50	EGCUT_WGS	ss3666171068	Jul 13, 2019 (153)
51	EVA_DECODE	ss3716243494	Jul 13, 2019 (153)
52	ACPOP	ss3733052810	Jul 13, 2019 (153)
53	EVA	ss3764405023	Jul 13, 2019 (153)
54	PACBIO	ss3785323302	Jul 13, 2019 (153)
55	PACBIO	ss3790694928	Jul 13, 2019 (153)
56	PACBIO	ss3795572053	Jul 13, 2019 (153)
57	KHV_HUMAN_GENOMES	ss3807567110	Jul 13, 2019 (153)
58	EVA	ss3829641347	Apr 26, 2020 (154)
59	EVA	ss3838293776	Apr 26, 2020 (154)
60	EVA	ss3843737662	Apr 26, 2020 (154)
61	SGDP_PRJ	ss3863547517	Apr 26, 2020 (154)
62	KRGDB	ss3910256172	Apr 26, 2020 (154)
63	KOGIC	ss3958164092	Apr 26, 2020 (154)
64	TOPMED	ss4688331046	Apr 26, 2021 (155)
65	TOMMO_GENOMICS	ss5175387362	Apr 26, 2021 (155)
66	1000G_HIGH_COVERAGE	ss5266805852	Oct 13, 2022 (156)
67	EVA	ss5362749807	Oct 13, 2022 (156)
68	HUGCELL_USP	ss5464676631	Oct 13, 2022 (156)
69	EVA	ss5508305441	Oct 13, 2022 (156)
70	1000G_HIGH_COVERAGE	ss5551958468	Oct 13, 2022 (156)
71	SANFORD_IMAGENETICS	ss5639426405	Oct 13, 2022 (156)
72	TOMMO_GENOMICS	ss5712822431	Oct 13, 2022 (156)
73	YY_MCH	ss5807000707	Oct 13, 2022 (156)
74	EVA	ss5836018867	Oct 13, 2022 (156)
75	EVA	ss5855129910	Oct 13, 2022 (156)
76	EVA	ss5897444296	Oct 13, 2022 (156)
77	EVA	ss5967926070	Oct 13, 2022 (156)
78	1000Genomes	NC_000005.9 - 170153389	Oct 12, 2018 (152)
79	1000Genomes_30x	NC_000005.10 - 170726385	Oct 13, 2022 (156)
80	The Avon Longitudinal Study of Parents and Children	NC_000005.9 - 170153389	Oct 12, 2018 (152)
81	Genetic variation in the Estonian population	NC_000005.9 - 170153389	Oct 12, 2018 (152)
82	The Danish reference pan genome	NC_000005.9 - 170153389	Apr 26, 2020 (154)
83	gnomAD - Genomes	NC_000005.10 - 170726385	Apr 26, 2021 (155)
84	Genome of the Netherlands Release 5	NC_000005.9 - 170153389	Apr 26, 2020 (154)
85	HapMap	NC_000005.10 - 170726385	Apr 26, 2020 (154)
86	KOREAN population from KRGDB	NC_000005.9 - 170153389	Apr 26, 2020 (154)
87	Korean Genome Project	NC_000005.10 - 170726385	Apr 26, 2020 (154)
88	Northern Sweden	NC_000005.9 - 170153389	Jul 13, 2019 (153)
89	Qatari	NC_000005.9 - 170153389	Apr 26, 2020 (154)
90	SGDP_PRJ	NC_000005.9 - 170153389	Apr 26, 2020 (154)
91	Siberian	NC_000005.9 - 170153389	Apr 26, 2020 (154)
92	8.3KJPN	NC_000005.9 - 170153389	Apr 26, 2021 (155)
93	14KJPN	NC_000005.10 - 170726385	Oct 13, 2022 (156)
94	TopMed	NC_000005.10 - 170726385	Apr 26, 2021 (155)
95	UK 10K study - Twins	NC_000005.9 - 170153389	Oct 12, 2018 (152)
96	A Vietnamese Genetic Variation Database	NC_000005.9 - 170153389	Jul 13, 2019 (153)
97	ALFA	NC_000005.10 - 170726385	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)
rs10393706	Sep 24, 2004 (123)
rs58965022	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
17433566, ss3910256172	NC_000005.9:170153388:T:A	NC_000005.10:170726384:T:A	(self)
4341493588	NC_000005.10:170726384:T:A	NC_000005.10:170726384:T:A	(self)
ss83665282, ss83959795, ss93333694, ss109622034, ss113657407, ss116906412, ss162887095, ss166228365, ss167363022, ss201203372, ss206706825, ss253946274, ss278585720, ss285308475, ss293520240, ss1591951872	NC_000005.8:170085966:T:C	NC_000005.10:170726384:T:C	(self)
30035139, 16722288, 11909316, 7626526, 7421783, 17433566, 6337675, 7700815, 15564497, 4119296, 33356669, 16722288, 3705936, ss222115457, ss233255751, ss240356424, ss558887643, ss652797546, ss982409315, ss1073255739, ss1318317689, ss1430582415, ss1581461587, ss1614606843, ss1657600876, ss1804199805, ss1925658885, ss1970271001, ss2023443173, ss2151602942, ss2626209758, ss2707179326, ss2833922658, ss2998233502, ss3346750929, ss3666171068, ss3733052810, ss3764405023, ss3785323302, ss3790694928, ss3795572053, ss3829641347, ss3838293776, ss3863547517, ss3910256172, ss5175387362, ss5362749807, ss5508305441, ss5639426405, ss5836018867, ss5967926070	NC_000005.9:170153388:T:C	NC_000005.10:170726384:T:C	(self)
39484403, 212432531, 3026174, 14542093, 46659535, 525708603, 4341493588, ss2280477446, ss3025504502, ss3648227204, ss3716243494, ss3807567110, ss3843737662, ss3958164092, ss4688331046, ss5266805852, ss5464676631, ss5551958468, ss5712822431, ss5807000707, ss5855129910, ss5897444296	NC_000005.10:170726384:T:C	NC_000005.10:170726384:T:C	(self)
ss14641829, ss14814085, ss17086438	NT_023133.11:14962946:T:C	NC_000005.10:170726384:T:C	(self)
ss2228495, ss42528650, ss105969163, ss143617711, ss156333222	NT_023133.13:14964661:T:C	NC_000005.10:170726384:T:C	(self)
17433566, ss3910256172	NC_000005.9:170153388:T:G	NC_000005.10:170726384: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 rs1422978

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.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1422978