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rs794728475

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs794728475(-;T)
Make rs794728475(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150974936
GeneKCNH2, LOC107986861
is asnp
is mentioned by
dbSNPrs794728475
dbSNP (old)rs794728475
ClinGenrs794728475
ebirs794728475
HLIrs794728475
Exacrs794728475
Varsomers794728475
Maprs794728475
PheGenIrs794728475
Biobankrs794728475
1000 genomesrs794728475
hgdprs794728475
ensemblrs794728475
gopubmedrs794728475
geneviewrs794728475
scholarrs794728475
googlers794728475
pharmgkbrs794728475
gwascentralrs794728475
openSNPrs794728475
23andMers794728475
23andMe allrs794728475
SNP Nexus

SNPshotrs794728475
SNPdbers794728475
MSV3drs794728475
GWAS Ctlgrs794728475
Max Magnitude0
ClinVar
Risk rs794728475(T;T)
Alt rs794728475(T;T)
Reference Rs794728475(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150672025dupA
CLNSRC
CLNACC RCV000182015.2,