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rs768286281

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs768286281(A;T)
Make rs768286281(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32822595
GenePKP2
is asnp
is mentioned by
dbSNPrs768286281
ebirs768286281
HLIrs768286281
Exacrs768286281
Varsomers768286281
Maprs768286281
PheGenIrs768286281
hapmaprs768286281
1000 genomesrs768286281
hgdprs768286281
ensemblrs768286281
gopubmedrs768286281
geneviewrs768286281
scholarrs768286281
googlers768286281
pharmgkbrs768286281
gwascentralrs768286281
openSNPrs768286281
23andMers768286281
23andMe allrs768286281
SNP Nexus

SNPshotrs768286281
SNPdbers768286281
MSV3drs768286281
GWAS Ctlgrs768286281
Max Magnitude0
ClinVar
Risk rs768286281(T;T)
Alt rs768286281(T;T)
Reference rs768286281(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.32975529A>T
CLNSRC
CLNACC RCV000183808.1,