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rs794728364

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728364(C;T)
Make rs794728364(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150957323
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728364
ebirs794728364
HLIrs794728364
Exacrs794728364
Varsomers794728364
Maprs794728364
PheGenIrs794728364
hapmaprs794728364
1000 genomesrs794728364
hgdprs794728364
ensemblrs794728364
gopubmedrs794728364
geneviewrs794728364
scholarrs794728364
googlers794728364
pharmgkbrs794728364
gwascentralrs794728364
openSNPrs794728364
23andMers794728364
23andMe allrs794728364
SNP Nexus

SNPshotrs794728364
SNPdbers794728364
MSV3drs794728364
GWAS Ctlgrs794728364
Max Magnitude0
ClinVar
Risk rs794728364(T;T)
Alt rs794728364(T;T)
Reference rs794728364(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150654411G>A
CLNSRC
CLNACC RCV000181779.2,