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rs794729119

From SNPedia

Orientationminus
Make rs794729119(-;-)
Make rs794729119(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32879016
GenePKP2
is asnp
is mentioned by
dbSNPrs794729119
ebirs794729119
HLIrs794729119
Exacrs794729119
Varsomers794729119
Maprs794729119
PheGenIrs794729119
hapmaprs794729119
1000 genomesrs794729119
hgdprs794729119
ensemblrs794729119
gopubmedrs794729119
geneviewrs794729119
scholarrs794729119
googlers794729119
pharmgkbrs794729119
gwascentralrs794729119
openSNPrs794729119
23andMers794729119
23andMe allrs794729119
SNP Nexus

SNPshotrs794729119
SNPdbers794729119
MSV3drs794729119
GWAS Ctlgrs794729119
Max Magnitude
ClinVar
Risk rs794729119(;)
Alt rs794729119(;)
Reference rs794729119(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.33031950delG
CLNSRC
CLNACC RCV000183779.1,