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rs794728483

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728483(A;A)
Make rs794728483(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150951651
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728483
ebirs794728483
HLIrs794728483
Exacrs794728483
Varsomers794728483
Maprs794728483
PheGenIrs794728483
hapmaprs794728483
1000 genomesrs794728483
hgdprs794728483
ensemblrs794728483
gopubmedrs794728483
geneviewrs794728483
scholarrs794728483
googlers794728483
pharmgkbrs794728483
gwascentralrs794728483
openSNPrs794728483
23andMers794728483
23andMe allrs794728483
SNP Nexus

SNPshotrs794728483
SNPdbers794728483
MSV3drs794728483
GWAS Ctlgrs794728483
Max Magnitude0
ClinVar
Risk rs794728483(A;A)
Alt rs794728483(A;A)
Reference rs794728483(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150648739G>T
CLNSRC
CLNACC RCV000182028.1,