rs786205817

Orientation

plus

Stabilized

plus

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

Make rs786205817(A;T)

Make rs786205817(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

70175935

Gene

KCNJ2

is a	snp
is	mentioned by
dbSNP	rs786205817
dbSNP (classic)	rs786205817
ClinGen	rs786205817
ebi	rs786205817
HLI	rs786205817
Exac	rs786205817
Gnomad	rs786205817
Varsome	rs786205817
LitVar	rs786205817
Map	rs786205817
PheGenI	rs786205817
Biobank	rs786205817
1000 genomes	rs786205817
hgdp	rs786205817
ensembl	rs786205817
geneview	rs786205817
scholar	rs786205817
google	rs786205817
pharmgkb	rs786205817
gwascentral	rs786205817
openSNP	rs786205817
23andMe	rs786205817
SNPshot	rs786205817
SNPdbe	rs786205817
MSV3d	rs786205817
GWAS Ctlg	rs786205817

Max Magnitude

0

ClinVar
Risk	rs786205817(T;T)
Alt	rs786205817(T;T)
Reference	Rs786205817(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNJ2
CLNDBN	not provided
Reversed	0
HGVS	NC_000017.10:g.68172076A>T
CLNSRC
CLNACC	RCV000170986.3,