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rs794728418

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728418(A;A)
Make rs794728418(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150977870
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728418
ebirs794728418
HLIrs794728418
Exacrs794728418
Varsomers794728418
Maprs794728418
PheGenIrs794728418
hapmaprs794728418
1000 genomesrs794728418
hgdprs794728418
ensemblrs794728418
gopubmedrs794728418
geneviewrs794728418
scholarrs794728418
googlers794728418
pharmgkbrs794728418
gwascentralrs794728418
openSNPrs794728418
23andMers794728418
23andMe allrs794728418
SNP Nexus

SNPshotrs794728418
SNPdbers794728418
MSV3drs794728418
GWAS Ctlgrs794728418
Max Magnitude0
ClinVar
Risk rs794728418(A;A)
Alt rs794728418(A;A)
Reference rs794728418(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150674958A>T
CLNSRC
CLNACC RCV000181954.1,