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rs794728371

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728371(C;T)
Make rs794728371(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150952463
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728371
ebirs794728371
HLIrs794728371
Exacrs794728371
Varsomers794728371
Maprs794728371
PheGenIrs794728371
hapmaprs794728371
1000 genomesrs794728371
hgdprs794728371
ensemblrs794728371
gopubmedrs794728371
geneviewrs794728371
scholarrs794728371
googlers794728371
pharmgkbrs794728371
gwascentralrs794728371
openSNPrs794728371
23andMers794728371
23andMe allrs794728371
SNP Nexus

SNPshotrs794728371
SNPdbers794728371
MSV3drs794728371
GWAS Ctlgrs794728371
Max Magnitude0
ClinVar
Risk rs794728371(T;T)
Alt rs794728371(T;T)
Reference rs794728371(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150649551G>A
CLNSRC
CLNACC RCV000181796.2,