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rs794728366

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728366(A;A)
Make rs794728366(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150952789
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728366
ebirs794728366
HLIrs794728366
Exacrs794728366
Varsomers794728366
Maprs794728366
PheGenIrs794728366
hapmaprs794728366
1000 genomesrs794728366
hgdprs794728366
ensemblrs794728366
gopubmedrs794728366
geneviewrs794728366
scholarrs794728366
googlers794728366
pharmgkbrs794728366
gwascentralrs794728366
openSNPrs794728366
23andMers794728366
23andMe allrs794728366
SNP Nexus

SNPshotrs794728366
SNPdbers794728366
MSV3drs794728366
GWAS Ctlgrs794728366
Max Magnitude0
ClinVar
Risk rs794728366(A;A)
Alt rs794728366(A;A)
Reference rs794728366(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150649877C>T
CLNSRC
CLNACC RCV000181782.2,