Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057520726

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520726(C;C)
Make rs1057520726(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position32821355
GenePKP2
is asnp
is mentioned by
dbSNPrs1057520726
dbSNP (old)rs1057520726
ClinGenrs1057520726
ebirs1057520726
HLIrs1057520726
Exacrs1057520726
Gnomadrs1057520726
Varsomers1057520726
LitVarrs1057520726
Maprs1057520726
PheGenIrs1057520726
Biobankrs1057520726
1000 genomesrs1057520726
hgdprs1057520726
ensemblrs1057520726
gopubmedrs1057520726
geneviewrs1057520726
scholarrs1057520726
googlers1057520726
pharmgkbrs1057520726
gwascentralrs1057520726
openSNPrs1057520726
23andMers1057520726
23andMe allrs1057520726
SNPshotrs1057520726
SNPdbers1057520726
MSV3drs1057520726
GWAS Ctlgrs1057520726
Max Magnitude0
ClinVar
Risk rs1057520726(C;C)
Alt rs1057520726(C;C)
Reference Rs1057520726(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.32974289C>G
CLNSRC
CLNACC RCV000425852.1,