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rs794728390

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728390(C;C)
Make rs794728390(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150950170
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728390
ebirs794728390
HLIrs794728390
Exacrs794728390
Varsomers794728390
Maprs794728390
PheGenIrs794728390
hapmaprs794728390
1000 genomesrs794728390
hgdprs794728390
ensemblrs794728390
gopubmedrs794728390
geneviewrs794728390
scholarrs794728390
googlers794728390
pharmgkbrs794728390
gwascentralrs794728390
openSNPrs794728390
23andMers794728390
23andMe allrs794728390
SNP Nexus

SNPshotrs794728390
SNPdbers794728390
MSV3drs794728390
GWAS Ctlgrs794728390
Max Magnitude0
ClinVar
Risk rs794728390(C;C)
Alt rs794728390(C;C)
Reference rs794728390(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150647258A>G
CLNSRC
CLNACC RCV000181857.2,