rs786205813

Orientation

plus

Stabilized

plus

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

Make rs786205813(C;C)

Make rs786205813(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

70175275

Gene

KCNJ2

is a	snp
is	mentioned by
dbSNP	rs786205813
dbSNP (classic)	rs786205813
ClinGen	rs786205813
ebi	rs786205813
HLI	rs786205813
Exac	rs786205813
Gnomad	rs786205813
Varsome	rs786205813
LitVar	rs786205813
Map	rs786205813
PheGenI	rs786205813
Biobank	rs786205813
1000 genomes	rs786205813
hgdp	rs786205813
ensembl	rs786205813
geneview	rs786205813
scholar	rs786205813
google	rs786205813
pharmgkb	rs786205813
gwascentral	rs786205813
openSNP	rs786205813
23andMe	rs786205813
SNPshot	rs786205813
SNPdbe	rs786205813
MSV3d	rs786205813
GWAS Ctlg	rs786205813

Max Magnitude

0

ClinVar
Risk	rs786205813(C;C)
Alt	rs786205813(C;C)
Reference	Rs786205813(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNJ2
CLNDBN	not provided
Reversed	0
HGVS	NC_000017.10:g.68171416T>C
CLNSRC
CLNACC	RCV000170975.2,