rs796052606

Orientation

minus

Stabilized

minus

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

Make rs796052606(G;T)

Make rs796052606(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

160070021

Gene	KCNJ10, KCNJ9

is a	snp
is	mentioned by
dbSNP	rs796052606
dbSNP (classic)	rs796052606
ClinGen	rs796052606
ebi	rs796052606
HLI	rs796052606
Exac	rs796052606
Gnomad	rs796052606
Varsome	rs796052606
LitVar	rs796052606
Map	rs796052606
PheGenI	rs796052606
Biobank	rs796052606
1000 genomes	rs796052606
hgdp	rs796052606
ensembl	rs796052606
geneview	rs796052606
scholar	rs796052606
google	rs796052606
pharmgkb	rs796052606
gwascentral	rs796052606
openSNP	rs796052606
23andMe	rs796052606
SNPshot	rs796052606
SNPdbe	rs796052606
MSV3d	rs796052606
GWAS Ctlg	rs796052606

Max Magnitude

0

ClinVar
Risk	rs796052606(A;A) rs796052606(T;T)
Alt	rs796052606(A;A) rs796052606(T;T)
Reference	Rs796052606(G;G)
Significance	Probable-Pathogenic
Disease	not provided not specified
Variation	info
Gene	KCNJ10
CLNDBN	not provided not specified
Reversed	1
HGVS	NC_000001.10:g.160039811C>A; NC_000001.10:g.160039811C>T
CLNSRC
CLNACC	RCV000187813.3, RCV000421213.1,