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rs794728488

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728488(A;C)
Make rs794728488(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150951122
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728488
ebirs794728488
HLIrs794728488
Exacrs794728488
Varsomers794728488
Maprs794728488
PheGenIrs794728488
hapmaprs794728488
1000 genomesrs794728488
hgdprs794728488
ensemblrs794728488
gopubmedrs794728488
geneviewrs794728488
scholarrs794728488
googlers794728488
pharmgkbrs794728488
gwascentralrs794728488
openSNPrs794728488
23andMers794728488
23andMe allrs794728488
SNP Nexus

SNPshotrs794728488
SNPdbers794728488
MSV3drs794728488
GWAS Ctlgrs794728488
Max Magnitude0
ClinVar
Risk rs794728488(C;C)
Alt rs794728488(C;C)
Reference rs794728488(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150648210T>G
CLNSRC
CLNACC RCV000182039.1,