rs786205811

Orientation

plus

Stabilized

plus

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

Make rs786205811(C;T)

Make rs786205811(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

70175157

Gene

KCNJ2

is a	snp
is	mentioned by
dbSNP	rs786205811
dbSNP (classic)	rs786205811
ClinGen	rs786205811
ebi	rs786205811
HLI	rs786205811
Exac	rs786205811
Gnomad	rs786205811
Varsome	rs786205811
LitVar	rs786205811
Map	rs786205811
PheGenI	rs786205811
Biobank	rs786205811
1000 genomes	rs786205811
hgdp	rs786205811
ensembl	rs786205811
geneview	rs786205811
scholar	rs786205811
google	rs786205811
pharmgkb	rs786205811
gwascentral	rs786205811
openSNP	rs786205811
23andMe	rs786205811
SNPshot	rs786205811
SNPdbe	rs786205811
MSV3d	rs786205811
GWAS Ctlg	rs786205811

Max Magnitude

0

ClinVar
Risk	rs786205811(T;T)
Alt	rs786205811(T;T)
Reference	Rs786205811(C;C)
Significance	Pathogenic
Disease	not specified
Variation	info
Gene	KCNJ2
CLNDBN	not specified
Reversed	0
HGVS	NC_000017.10:g.68171298C>T
CLNSRC
CLNACC	RCV000170970.3,