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rs794728377

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728377(A;G)
Make rs794728377(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150951493
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728377
ebirs794728377
HLIrs794728377
Exacrs794728377
Varsomers794728377
Maprs794728377
PheGenIrs794728377
hapmaprs794728377
1000 genomesrs794728377
hgdprs794728377
ensemblrs794728377
gopubmedrs794728377
geneviewrs794728377
scholarrs794728377
googlers794728377
pharmgkbrs794728377
gwascentralrs794728377
openSNPrs794728377
23andMers794728377
23andMe allrs794728377
SNP Nexus

SNPshotrs794728377
SNPdbers794728377
MSV3drs794728377
GWAS Ctlgrs794728377
Max Magnitude0
ClinVar
Risk rs794728377(G;G)
Alt rs794728377(G;G)
Reference rs794728377(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150648581T>C
CLNSRC
CLNACC RCV000181826.1,