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rs370637245

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs370637245(C;T)
Make rs370637245(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150952457
GeneKCNH2
is asnp
is mentioned by
dbSNPrs370637245
ebirs370637245
HLIrs370637245
Exacrs370637245
Varsomers370637245
Maprs370637245
PheGenIrs370637245
hapmaprs370637245
1000 genomesrs370637245
hgdprs370637245
ensemblrs370637245
gopubmedrs370637245
geneviewrs370637245
scholarrs370637245
googlers370637245
pharmgkbrs370637245
gwascentralrs370637245
openSNPrs370637245
23andMers370637245
23andMe allrs370637245
SNP Nexus

SNPshotrs370637245
SNPdbers370637245
MSV3drs370637245
GWAS Ctlgrs370637245
Max Magnitude0
ClinVar
Risk rs370637245(T;T)
Alt rs370637245(T;T)
Reference rs370637245(C;C)
Significance Probable-Pathogenic
Disease Cardiac arrhythmia
Variation info
Gene KCNH2
CLNDBN Cardiac arrhythmia
Reversed 0
HGVS NC_000007.13:g.150649545C>T
CLNSRC
CLNACC RCV000181798.1,