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rs794728414

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728414(A;C)
Make rs794728414(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150974734
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728414
ebirs794728414
HLIrs794728414
Exacrs794728414
Varsomers794728414
Maprs794728414
PheGenIrs794728414
hapmaprs794728414
1000 genomesrs794728414
hgdprs794728414
ensemblrs794728414
gopubmedrs794728414
geneviewrs794728414
scholarrs794728414
googlers794728414
pharmgkbrs794728414
gwascentralrs794728414
openSNPrs794728414
23andMers794728414
23andMe allrs794728414
SNP Nexus

SNPshotrs794728414
SNPdbers794728414
MSV3drs794728414
GWAS Ctlgrs794728414
Max Magnitude0
ClinVar
Risk rs794728414(C;C)
Alt rs794728414(C;C)
Reference rs794728414(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150671822T>G
CLNSRC
CLNACC RCV000181945.2,