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rs794728432

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs794728432(-;C)
Make rs794728432(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150952849
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728432
dbSNP (old)rs794728432
ClinGenrs794728432
ebirs794728432
HLIrs794728432
Exacrs794728432
Gnomadrs794728432
Varsomers794728432
Maprs794728432
PheGenIrs794728432
Biobankrs794728432
1000 genomesrs794728432
hgdprs794728432
ensemblrs794728432
gopubmedrs794728432
geneviewrs794728432
scholarrs794728432
googlers794728432
pharmgkbrs794728432
gwascentralrs794728432
openSNPrs794728432
23andMers794728432
23andMe allrs794728432
SNP Nexus

SNPshotrs794728432
SNPdbers794728432
MSV3drs794728432
GWAS Ctlgrs794728432
Max Magnitude0
ClinVar
Risk rs794728432(C;C)
Alt rs794728432(C;C)
Reference Rs794728432(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150649938dupG
CLNSRC
CLNACC RCV000181970.2,