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rs794728484

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728484(G;T)
Make rs794728484(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150951639
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728484
ebirs794728484
HLIrs794728484
Exacrs794728484
Varsomers794728484
Maprs794728484
PheGenIrs794728484
hapmaprs794728484
1000 genomesrs794728484
hgdprs794728484
ensemblrs794728484
gopubmedrs794728484
geneviewrs794728484
scholarrs794728484
googlers794728484
pharmgkbrs794728484
gwascentralrs794728484
openSNPrs794728484
23andMers794728484
23andMe allrs794728484
SNP Nexus

SNPshotrs794728484
SNPdbers794728484
MSV3drs794728484
GWAS Ctlgrs794728484
Max Magnitude0
ClinVar
Risk rs794728484(T;T)
Alt rs794728484(T;T)
Reference rs794728484(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150648727C>A
CLNSRC
CLNACC RCV000182029.1,