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rs794728365

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728365(A;G)
Make rs794728365(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150952855
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728365
ebirs794728365
HLIrs794728365
Exacrs794728365
Varsomers794728365
Maprs794728365
PheGenIrs794728365
hapmaprs794728365
1000 genomesrs794728365
hgdprs794728365
ensemblrs794728365
gopubmedrs794728365
geneviewrs794728365
scholarrs794728365
googlers794728365
pharmgkbrs794728365
gwascentralrs794728365
openSNPrs794728365
23andMers794728365
23andMe allrs794728365
SNP Nexus

SNPshotrs794728365
SNPdbers794728365
MSV3drs794728365
GWAS Ctlgrs794728365
Max Magnitude0
ClinVar
Risk rs794728365(G;G)
Alt rs794728365(G;G)
Reference rs794728365(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150649943T>C
CLNSRC
CLNACC RCV000181781.1,