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rs794729128

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
(I;I) 0 common genotype
Make rs794729128(-;-)
Make rs794729128(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32824052
GenePKP2
is asnp
is mentioned by
dbSNPrs794729128
dbSNP (classic)rs794729128
ClinGenrs794729128
ebirs794729128
HLIrs794729128
Exacrs794729128
Gnomadrs794729128
Varsomers794729128
LitVarrs794729128
Maprs794729128
PheGenIrs794729128
Biobankrs794729128
1000 genomesrs794729128
hgdprs794729128
ensemblrs794729128
geneviewrs794729128
scholarrs794729128
googlers794729128
pharmgkbrs794729128
gwascentralrs794729128
openSNPrs794729128
23andMers794729128
SNPshotrs794729128
SNPdbers794729128
MSV3drs794729128
GWAS Ctlgrs794729128
Max Magnitude0
ClinVar
Risk rs794729128(-;-)
Alt rs794729128(-;-)
Reference Rs794729128(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.32976986delT
CLNSRC
CLNACC RCV000183793.1,