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rs794728352

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728352(C;T)
Make rs794728352(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150959665
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728352
ebirs794728352
HLIrs794728352
Exacrs794728352
Varsomers794728352
Maprs794728352
PheGenIrs794728352
hapmaprs794728352
1000 genomesrs794728352
hgdprs794728352
ensemblrs794728352
gopubmedrs794728352
geneviewrs794728352
scholarrs794728352
googlers794728352
pharmgkbrs794728352
gwascentralrs794728352
openSNPrs794728352
23andMers794728352
23andMe allrs794728352
SNP Nexus

SNPshotrs794728352
SNPdbers794728352
MSV3drs794728352
GWAS Ctlgrs794728352
Max Magnitude0
ClinVar
Risk rs794728352(T;T)
Alt rs794728352(T;T)
Reference rs794728352(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150656753G>A
CLNSRC
CLNACC RCV000181753.1,