rs121912243

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs121912243(C;T)

Make rs121912243(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

20

Position

63350969

Gene

CHRNA4

is a	snp
is	mentioned by
dbSNP	rs121912243
dbSNP (classic)	rs121912243
ClinGen	rs121912243
ebi	rs121912243
HLI	rs121912243
Exac	rs121912243
Gnomad	rs121912243
Varsome	rs121912243
LitVar	rs121912243
Map	rs121912243
PheGenI	rs121912243
Biobank	rs121912243
1000 genomes	rs121912243
hgdp	rs121912243
ensembl	rs121912243
geneview	rs121912243
scholar	rs121912243
google	rs121912243
pharmgkb	rs121912243
gwascentral	rs121912243
openSNP	rs121912243
23andMe	rs121912243
SNPshot	rs121912243
SNPdbe	rs121912243
MSV3d	rs121912243
GWAS Ctlg	rs121912243

Max Magnitude

0

ClinVar
Risk	rs121912243(T;T)
Alt	rs121912243(T;T)
Reference	Rs121912243(C;C)
Significance	Probable-Pathogenic
Disease	Tobacco use disorder not specified Inborn genetic diseases
Variation	info
Gene	CHRNA4
CLNDBN	Tobacco use disorder not specified Inborn genetic diseases
Reversed	1
HGVS	NC_000020.10:g.61982321G>A
CLNSRC
CLNACC	RCV000084614.1, RCV000186922.2, RCV000190688.1,