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rs794728385

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728385(A;C)
Make rs794728385(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150950374
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728385
ebirs794728385
HLIrs794728385
Exacrs794728385
Varsomers794728385
Maprs794728385
PheGenIrs794728385
hapmaprs794728385
1000 genomesrs794728385
hgdprs794728385
ensemblrs794728385
gopubmedrs794728385
geneviewrs794728385
scholarrs794728385
googlers794728385
pharmgkbrs794728385
gwascentralrs794728385
openSNPrs794728385
23andMers794728385
23andMe allrs794728385
SNP Nexus

SNPshotrs794728385
SNPdbers794728385
MSV3drs794728385
GWAS Ctlgrs794728385
Max Magnitude0
ClinVar
Risk rs794728385(C;C)
Alt rs794728385(C;C)
Reference rs794728385(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150647462T>G
CLNSRC
CLNACC RCV000181841.1,