rs1057517866

Orientation

minus

Stabilized

minus

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

Make rs1057517866(A;A)

Make rs1057517866(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

150951729

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs1057517866
dbSNP (classic)	rs1057517866
ClinGen	rs1057517866
ebi	rs1057517866
HLI	rs1057517866
Exac	rs1057517866
Gnomad	rs1057517866
Varsome	rs1057517866
LitVar	rs1057517866
Map	rs1057517866
PheGenI	rs1057517866
Biobank	rs1057517866
1000 genomes	rs1057517866
hgdp	rs1057517866
ensembl	rs1057517866
geneview	rs1057517866
scholar	rs1057517866
google	rs1057517866
pharmgkb	rs1057517866
gwascentral	rs1057517866
openSNP	rs1057517866
23andMe	rs1057517866
SNPshot	rs1057517866
SNPdbe	rs1057517866
MSV3d	rs1057517866
GWAS Ctlg	rs1057517866

Max Magnitude

0

ClinVar
Risk	rs1057517866(A;A)
Alt	rs1057517866(A;A)
Reference	Rs1057517866(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150648817C>T
CLNSRC
CLNACC	RCV000412811.1,