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rs794728478

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728478(A;A)
Make rs794728478(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150952854
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728478
ebirs794728478
HLIrs794728478
Exacrs794728478
Varsomers794728478
Maprs794728478
PheGenIrs794728478
hapmaprs794728478
1000 genomesrs794728478
hgdprs794728478
ensemblrs794728478
gopubmedrs794728478
geneviewrs794728478
scholarrs794728478
googlers794728478
pharmgkbrs794728478
gwascentralrs794728478
openSNPrs794728478
23andMers794728478
23andMe allrs794728478
SNP Nexus

SNPshotrs794728478
SNPdbers794728478
MSV3drs794728478
GWAS Ctlgrs794728478
Max Magnitude0
ClinVar
Risk rs794728478(A;A)
Alt rs794728478(A;A)
Reference rs794728478(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150649942C>T
CLNSRC
CLNACC RCV000182018.1,