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rs794728407

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728407(C;T)
Make rs794728407(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150974899
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728407
ebirs794728407
HLIrs794728407
Exacrs794728407
Varsomers794728407
Maprs794728407
PheGenIrs794728407
hapmaprs794728407
1000 genomesrs794728407
hgdprs794728407
ensemblrs794728407
gopubmedrs794728407
geneviewrs794728407
scholarrs794728407
googlers794728407
pharmgkbrs794728407
gwascentralrs794728407
openSNPrs794728407
23andMers794728407
23andMe allrs794728407
SNP Nexus

SNPshotrs794728407
SNPdbers794728407
MSV3drs794728407
GWAS Ctlgrs794728407
Max Magnitude0
ClinVar
Risk rs794728407(T;T)
Alt rs794728407(T;T)
Reference rs794728407(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150671987G>A
CLNSRC
CLNACC RCV000181924.1,