rs199473024

Orientation

minus

Stabilized

minus

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

Make rs199473024(A;G)

Make rs199473024(G;G)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150947362

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199473024
dbSNP (classic)	rs199473024
ClinGen	rs199473024
ebi	rs199473024
HLI	rs199473024
Exac	rs199473024
Gnomad	rs199473024
Varsome	rs199473024
LitVar	rs199473024
Map	rs199473024
PheGenI	rs199473024
Biobank	rs199473024
1000 genomes	rs199473024
hgdp	rs199473024
ensembl	rs199473024
geneview	rs199473024
scholar	rs199473024
google	rs199473024
pharmgkb	rs199473024
gwascentral	rs199473024
openSNP	rs199473024
23andMe	rs199473024
SNPshot	rs199473024
SNPdbe	rs199473024
MSV3d	rs199473024
GWAS Ctlg	rs199473024

Max Magnitude

0

ClinVar
Risk	rs199473024(G;G)
Alt	rs199473024(G;G)
Reference	Rs199473024(A;A)
Significance	Untested
Disease	SUDDEN INFANT DEATH SYNDROME
Variation	info
Gene	KCNH2
CLNDBN	SUDDEN INFANT DEATH SYNDROME
Reversed	1
HGVS	NC_000007.13:g.150644450T>C
CLNSRC	ClinVar
CLNACC	RCV000058200.3,