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rs794728482

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728482(C;T)
Make rs794728482(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150951699
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728482
ebirs794728482
HLIrs794728482
Exacrs794728482
Varsomers794728482
Maprs794728482
PheGenIrs794728482
hapmaprs794728482
1000 genomesrs794728482
hgdprs794728482
ensemblrs794728482
gopubmedrs794728482
geneviewrs794728482
scholarrs794728482
googlers794728482
pharmgkbrs794728482
gwascentralrs794728482
openSNPrs794728482
23andMers794728482
23andMe allrs794728482
SNP Nexus

SNPshotrs794728482
SNPdbers794728482
MSV3drs794728482
GWAS Ctlgrs794728482
Max Magnitude0
ClinVar
Risk rs794728482(T;T)
Alt rs794728482(T;T)
Reference rs794728482(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150648787G>A
CLNSRC
CLNACC RCV000182027.1,