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rs794728396

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728396(C;T)
Make rs794728396(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150948872
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728396
ebirs794728396
HLIrs794728396
Exacrs794728396
Varsomers794728396
Maprs794728396
PheGenIrs794728396
hapmaprs794728396
1000 genomesrs794728396
hgdprs794728396
ensemblrs794728396
gopubmedrs794728396
geneviewrs794728396
scholarrs794728396
googlers794728396
pharmgkbrs794728396
gwascentralrs794728396
openSNPrs794728396
23andMers794728396
23andMe allrs794728396
SNP Nexus

SNPshotrs794728396
SNPdbers794728396
MSV3drs794728396
GWAS Ctlgrs794728396
Max Magnitude0
ClinVar
Risk rs794728396(T;T)
Alt rs794728396(T;T)
Reference rs794728396(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150645960G>A
CLNSRC
CLNACC RCV000181875.1,