rs199473549

Orientation

minus

Stabilized

minus

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

Make rs199473549(G;T)

Make rs199473549(T;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150958094

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199473549
dbSNP (classic)	rs199473549
ClinGen	rs199473549
ebi	rs199473549
HLI	rs199473549
Exac	rs199473549
Gnomad	rs199473549
Varsome	rs199473549
LitVar	rs199473549
Map	rs199473549
PheGenI	rs199473549
Biobank	rs199473549
1000 genomes	rs199473549
hgdp	rs199473549
ensembl	rs199473549
geneview	rs199473549
scholar	rs199473549
google	rs199473549
pharmgkb	rs199473549
gwascentral	rs199473549
openSNP	rs199473549
23andMe	rs199473549
SNPshot	rs199473549
SNPdbe	rs199473549
MSV3d	rs199473549
GWAS Ctlg	rs199473549

Max Magnitude

0

ClinVar
Risk	rs199473549(T;T)
Alt	rs199473549(T;T)
Reference	Rs199473549(G;G)
Significance	Untested
Disease	SUDDEN INFANT DEATH SYNDROME
Variation	info
Gene	KCNH2
CLNDBN	SUDDEN INFANT DEATH SYNDROME
Reversed	1
HGVS	NC_000007.13:g.150655182C>A
CLNSRC	ClinVar
CLNACC	RCV000058268.3,