rs141401803

Orientation

plus

Stabilized

plus

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

Make rs141401803(A;A)

Make rs141401803(A;G)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150947711

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs141401803
dbSNP (classic)	rs141401803
ClinGen	rs141401803
ebi	rs141401803
HLI	rs141401803
Exac	rs141401803
Gnomad	rs141401803
Varsome	rs141401803
LitVar	rs141401803
Map	rs141401803
PheGenI	rs141401803
Biobank	rs141401803
1000 genomes	rs141401803
hgdp	rs141401803
ensembl	rs141401803
geneview	rs141401803
scholar	rs141401803
google	rs141401803
pharmgkb	rs141401803
gwascentral	rs141401803
openSNP	rs141401803
23andMe	rs141401803
SNPshot	rs141401803
SNPdbe	rs141401803
MSV3d	rs141401803
GWAS Ctlg	rs141401803

Max Magnitude

0

ClinVar
Risk	rs141401803(A;A)
Alt	rs141401803(A;A)
Reference	Rs141401803(G;G)
Significance	Probable-Pathogenic
Disease	SUDDEN INFANT DEATH SYNDROME not provided
Variation	info
Gene	KCNH2
CLNDBN	SUDDEN INFANT DEATH SYNDROME not provided
Reversed	0
HGVS	NC_000007.13:g.150644799G>A
CLNSRC	ClinVar
CLNACC	RCV000058171.3, RCV000181898.3,