rs1057517743

Orientation

minus

Stabilized

minus

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

Make rs1057517743(-;-)

Make rs1057517743(-;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

150947381

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs1057517743
dbSNP (classic)	rs1057517743
ClinGen	rs1057517743
ebi	rs1057517743
HLI	rs1057517743
Exac	rs1057517743
Gnomad	rs1057517743
Varsome	rs1057517743
LitVar	rs1057517743
Map	rs1057517743
PheGenI	rs1057517743
Biobank	rs1057517743
1000 genomes	rs1057517743
hgdp	rs1057517743
ensembl	rs1057517743
geneview	rs1057517743
scholar	rs1057517743
google	rs1057517743
pharmgkb	rs1057517743
gwascentral	rs1057517743
openSNP	rs1057517743
23andMe	rs1057517743
SNPshot	rs1057517743
SNPdbe	rs1057517743
MSV3d	rs1057517743
GWAS Ctlg	rs1057517743

Max Magnitude

0

ClinVar
Risk	rs1057517743(-;-)
Alt	rs1057517743(-;-)
Reference	Rs1057517743(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150644469delC
CLNSRC
CLNACC	RCV000414670.1,