rs786205818

Orientation

plus

Stabilized

plus

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

Make rs786205818(A;G)

Make rs786205818(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

70175940

Gene

KCNJ2

is a	snp
is	mentioned by
dbSNP	rs786205818
dbSNP (classic)	rs786205818
ClinGen	rs786205818
ebi	rs786205818
HLI	rs786205818
Exac	rs786205818
Gnomad	rs786205818
Varsome	rs786205818
LitVar	rs786205818
Map	rs786205818
PheGenI	rs786205818
Biobank	rs786205818
1000 genomes	rs786205818
hgdp	rs786205818
ensembl	rs786205818
geneview	rs786205818
scholar	rs786205818
google	rs786205818
pharmgkb	rs786205818
gwascentral	rs786205818
openSNP	rs786205818
23andMe	rs786205818
SNPshot	rs786205818
SNPdbe	rs786205818
MSV3d	rs786205818
GWAS Ctlg	rs786205818

Max Magnitude

0

ClinVar
Risk	rs786205818(C;C) rs786205818(G;G)
Alt	rs786205818(C;C) rs786205818(G;G)
Reference	Rs786205818(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNJ2
CLNDBN	not provided
Reversed	0
HGVS	NC_000017.10:g.68172081A>C; NC_000017.10:g.68172081A>G
CLNSRC
CLNACC	RCV000435544.1, RCV000170988.2,