rs1057520477

Orientation

minus

Stabilized

minus

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

Make rs1057520477(C;G)

Make rs1057520477(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

150951707

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs1057520477
dbSNP (classic)	rs1057520477
ClinGen	rs1057520477
ebi	rs1057520477
HLI	rs1057520477
Exac	rs1057520477
Gnomad	rs1057520477
Varsome	rs1057520477
LitVar	rs1057520477
Map	rs1057520477
PheGenI	rs1057520477
Biobank	rs1057520477
1000 genomes	rs1057520477
hgdp	rs1057520477
ensembl	rs1057520477
geneview	rs1057520477
scholar	rs1057520477
google	rs1057520477
pharmgkb	rs1057520477
gwascentral	rs1057520477
openSNP	rs1057520477
23andMe	rs1057520477
SNPshot	rs1057520477
SNPdbe	rs1057520477
MSV3d	rs1057520477
GWAS Ctlg	rs1057520477

Max Magnitude

0

ClinVar
Risk	rs1057520477(G;G)
Alt	rs1057520477(G;G)
Reference	Rs1057520477(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150648795G>C
CLNSRC
CLNACC	RCV000434772.1,