rs199473434

Orientation

minus

Stabilized

minus

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

Make rs199473434(C;T)

Make rs199473434(T;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150948452

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199473434
dbSNP (classic)	rs199473434
ClinGen	rs199473434
ebi	rs199473434
HLI	rs199473434
Exac	rs199473434
Gnomad	rs199473434
Varsome	rs199473434
LitVar	rs199473434
Map	rs199473434
PheGenI	rs199473434
Biobank	rs199473434
1000 genomes	rs199473434
hgdp	rs199473434
ensembl	rs199473434
geneview	rs199473434
scholar	rs199473434
google	rs199473434
pharmgkb	rs199473434
gwascentral	rs199473434
openSNP	rs199473434
23andMe	rs199473434
SNPshot	rs199473434
SNPdbe	rs199473434
MSV3d	rs199473434
GWAS Ctlg	rs199473434

Max Magnitude

0

ClinVar
Risk	rs199473434(G;G) rs199473434(T;T)
Alt	rs199473434(G;G) rs199473434(T;T)
Reference	Rs199473434(C;C)
Significance	Untested
Disease	SUDDEN INFANT DEATH SYNDROME
Variation	info
Gene	KCNH2
CLNDBN	SUDDEN INFANT DEATH SYNDROME
Reversed	1
HGVS	NC_000007.13:g.150645540G>A
CLNSRC	ClinVar
CLNACC	RCV000058151.3,