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rs141401803

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs141401803(A;A)
Make rs141401803(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150947711
GeneKCNH2
is asnp
is mentioned by
dbSNPrs141401803
ebirs141401803
HLIrs141401803
Exacrs141401803
Varsomers141401803
Maprs141401803
PheGenIrs141401803
hapmaprs141401803
1000 genomesrs141401803
hgdprs141401803
ensemblrs141401803
gopubmedrs141401803
geneviewrs141401803
scholarrs141401803
googlers141401803
pharmgkbrs141401803
gwascentralrs141401803
openSNPrs141401803
23andMers141401803
23andMe allrs141401803
SNP Nexus

SNPshotrs141401803
SNPdbers141401803
MSV3drs141401803
GWAS Ctlgrs141401803
Max Magnitude0
ClinVar
Risk rs141401803(A;A)
Alt rs141401803(A;A)
Reference rs141401803(G;G)
Significance 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 RCV000058171.2, RCV000181898.2,