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rs794728481

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728481(C;T)
Make rs794728481(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150951709
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728481
ebirs794728481
HLIrs794728481
Exacrs794728481
Varsomers794728481
Maprs794728481
PheGenIrs794728481
hapmaprs794728481
1000 genomesrs794728481
hgdprs794728481
ensemblrs794728481
gopubmedrs794728481
geneviewrs794728481
scholarrs794728481
googlers794728481
pharmgkbrs794728481
gwascentralrs794728481
openSNPrs794728481
23andMers794728481
23andMe allrs794728481
SNP Nexus

SNPshotrs794728481
SNPdbers794728481
MSV3drs794728481
GWAS Ctlgrs794728481
Max Magnitude0
ClinVar
Risk rs794728481(T;T)
Alt rs794728481(T;T)
Reference rs794728481(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150648797G>A
CLNSRC
CLNACC RCV000182026.1,