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rs1064796069

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CACTGGAT;CACTGGAT) 0 common in clinvar
Chromosome12
Position32841035
GenePKP2
is asnp
is mentioned by
dbSNPrs1064796069
dbSNP (classic)rs1064796069
ClinGenrs1064796069
ebirs1064796069
HLIrs1064796069
Exacrs1064796069
Gnomadrs1064796069
Varsomers1064796069
LitVarrs1064796069
Maprs1064796069
PheGenIrs1064796069
Biobankrs1064796069
1000 genomesrs1064796069
hgdprs1064796069
ensemblrs1064796069
geneviewrs1064796069
scholarrs1064796069
googlers1064796069
pharmgkbrs1064796069
gwascentralrs1064796069
openSNPrs1064796069
23andMers1064796069
SNPshotrs1064796069
SNPdbers1064796069
MSV3drs1064796069
GWAS Ctlgrs1064796069
Max Magnitude0
ClinVar
Risk rs1064796069(-;-)
Alt rs1064796069(-;-)
Reference Rs1064796069(CACTGGAT;CACTGGAT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.32993969_32993976delATCCAGTG
CLNSRC
CLNACC RCV000478327.1,