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rs794728368

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728368(C;C)
Make rs794728368(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150952700
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728368
ebirs794728368
HLIrs794728368
Exacrs794728368
Varsomers794728368
Maprs794728368
PheGenIrs794728368
hapmaprs794728368
1000 genomesrs794728368
hgdprs794728368
ensemblrs794728368
gopubmedrs794728368
geneviewrs794728368
scholarrs794728368
googlers794728368
pharmgkbrs794728368
gwascentralrs794728368
openSNPrs794728368
23andMers794728368
23andMe allrs794728368
SNP Nexus

SNPshotrs794728368
SNPdbers794728368
MSV3drs794728368
GWAS Ctlgrs794728368
Max Magnitude0
ClinVar
Risk rs794728368(C;C)
Alt rs794728368(C;C)
Reference rs794728368(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150649788A>G
CLNSRC
CLNACC RCV000181787.2,