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rs141117135

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs141117135(C;T)
Make rs141117135(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150947639
GeneKCNH2
is asnp
is mentioned by
dbSNPrs141117135
ebirs141117135
HLIrs141117135
Exacrs141117135
Varsomers141117135
Maprs141117135
PheGenIrs141117135
hapmaprs141117135
1000 genomesrs141117135
hgdprs141117135
ensemblrs141117135
gopubmedrs141117135
geneviewrs141117135
scholarrs141117135
googlers141117135
pharmgkbrs141117135
gwascentralrs141117135
openSNPrs141117135
23andMers141117135
23andMe allrs141117135
SNP Nexus

SNPshotrs141117135
SNPdbers141117135
MSV3drs141117135
GWAS Ctlgrs141117135
Max Magnitude0
ClinVar
Risk rs141117135(A,T;A,T)
Alt rs141117135(A,T;A,T)
Reference rs141117135(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.150644727C>A; NC_000007.13:g.150644727C>T
CLNSRC
CLNACC RCV000181885.2, RCV000058180.2,