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rs763639737

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs763639737(A;G)
Make rs763639737(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32878981
GenePKP2
is asnp
is mentioned by
dbSNPrs763639737
ebirs763639737
HLIrs763639737
Exacrs763639737
Varsomers763639737
Maprs763639737
PheGenIrs763639737
hapmaprs763639737
1000 genomesrs763639737
hgdprs763639737
ensemblrs763639737
gopubmedrs763639737
geneviewrs763639737
scholarrs763639737
googlers763639737
pharmgkbrs763639737
gwascentralrs763639737
openSNPrs763639737
23andMers763639737
23andMe allrs763639737
SNP Nexus

SNPshotrs763639737
SNPdbers763639737
MSV3drs763639737
GWAS Ctlgrs763639737
Max Magnitude0
ClinVar
Risk rs763639737(G;G)
Alt rs763639737(G;G)
Reference rs763639737(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.33031915A>T
CLNSRC
CLNACC RCV000183800.2,