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rs794728492

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728492(G;G)
Make rs794728492(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150950305
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728492
ebirs794728492
HLIrs794728492
Exacrs794728492
Varsomers794728492
Maprs794728492
PheGenIrs794728492
hapmaprs794728492
1000 genomesrs794728492
hgdprs794728492
ensemblrs794728492
gopubmedrs794728492
geneviewrs794728492
scholarrs794728492
googlers794728492
pharmgkbrs794728492
gwascentralrs794728492
openSNPrs794728492
23andMers794728492
23andMe allrs794728492
SNP Nexus

SNPshotrs794728492
SNPdbers794728492
MSV3drs794728492
GWAS Ctlgrs794728492
Max Magnitude0
ClinVar
Risk rs794728492(G;G)
Alt rs794728492(G;G)
Reference rs794728492(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150647393A>C
CLNSRC
CLNACC RCV000182044.1,