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rs794728406

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728406(A;A)
Make rs794728406(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150974942
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728406
ebirs794728406
HLIrs794728406
Exacrs794728406
Varsomers794728406
Maprs794728406
PheGenIrs794728406
hapmaprs794728406
1000 genomesrs794728406
hgdprs794728406
ensemblrs794728406
gopubmedrs794728406
geneviewrs794728406
scholarrs794728406
googlers794728406
pharmgkbrs794728406
gwascentralrs794728406
openSNPrs794728406
23andMers794728406
23andMe allrs794728406
SNP Nexus

SNPshotrs794728406
SNPdbers794728406
MSV3drs794728406
GWAS Ctlgrs794728406
Max Magnitude0
ClinVar
Risk rs794728406(A;A)
Alt rs794728406(A;A)
Reference rs794728406(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150672030C>T
CLNSRC
CLNACC RCV000181919.2,