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rs794728392

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728392(G;T)
Make rs794728392(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150950163
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728392
ebirs794728392
HLIrs794728392
Exacrs794728392
Varsomers794728392
Maprs794728392
PheGenIrs794728392
hapmaprs794728392
1000 genomesrs794728392
hgdprs794728392
ensemblrs794728392
gopubmedrs794728392
geneviewrs794728392
scholarrs794728392
googlers794728392
pharmgkbrs794728392
gwascentralrs794728392
openSNPrs794728392
23andMers794728392
23andMe allrs794728392
SNP Nexus

SNPshotrs794728392
SNPdbers794728392
MSV3drs794728392
GWAS Ctlgrs794728392
Max Magnitude0
ClinVar
Risk rs794728392(T;T)
Alt rs794728392(T;T)
Reference rs794728392(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150647251C>A
CLNSRC
CLNACC RCV000181859.2,