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rs794728375

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728375(A;A)
Make rs794728375(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150951121
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728375
ebirs794728375
HLIrs794728375
Exacrs794728375
Varsomers794728375
Maprs794728375
PheGenIrs794728375
hapmaprs794728375
1000 genomesrs794728375
hgdprs794728375
ensemblrs794728375
gopubmedrs794728375
geneviewrs794728375
scholarrs794728375
googlers794728375
pharmgkbrs794728375
gwascentralrs794728375
openSNPrs794728375
23andMers794728375
23andMe allrs794728375
SNP Nexus

SNPshotrs794728375
SNPdbers794728375
MSV3drs794728375
GWAS Ctlgrs794728375
Max Magnitude0
ClinVar
Risk rs794728375(A;A)
Alt rs794728375(A;A)
Reference rs794728375(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150648209C>T
CLNSRC
CLNACC RCV000181813.2,