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rs794728395

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728395(A;A)
Make rs794728395(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150948944
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728395
ebirs794728395
HLIrs794728395
Exacrs794728395
Varsomers794728395
Maprs794728395
PheGenIrs794728395
hapmaprs794728395
1000 genomesrs794728395
hgdprs794728395
ensemblrs794728395
gopubmedrs794728395
geneviewrs794728395
scholarrs794728395
googlers794728395
pharmgkbrs794728395
gwascentralrs794728395
openSNPrs794728395
23andMers794728395
23andMe allrs794728395
SNP Nexus

SNPshotrs794728395
SNPdbers794728395
MSV3drs794728395
GWAS Ctlgrs794728395
Max Magnitude0
ClinVar
Risk rs794728395(A;A)
Alt rs794728395(A;A)
Reference rs794728395(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150646032C>T
CLNSRC
CLNACC RCV000181871.1,