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rs794728381

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728381(C;T)
Make rs794728381(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150951040
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728381
ebirs794728381
HLIrs794728381
Exacrs794728381
Varsomers794728381
Maprs794728381
PheGenIrs794728381
hapmaprs794728381
1000 genomesrs794728381
hgdprs794728381
ensemblrs794728381
gopubmedrs794728381
geneviewrs794728381
scholarrs794728381
googlers794728381
pharmgkbrs794728381
gwascentralrs794728381
openSNPrs794728381
23andMers794728381
23andMe allrs794728381
SNP Nexus

SNPshotrs794728381
SNPdbers794728381
MSV3drs794728381
GWAS Ctlgrs794728381
Max Magnitude0
ClinVar
Risk rs794728381(T;T)
Alt rs794728381(T;T)
Reference rs794728381(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150648128G>A
CLNSRC
CLNACC RCV000181834.1,