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

rs774942476

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs774942476(A;A)
Make rs774942476(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32841133
GenePKP2
is asnp
is mentioned by
dbSNPrs774942476
ebirs774942476
HLIrs774942476
Exacrs774942476
Varsomers774942476
Maprs774942476
PheGenIrs774942476
hapmaprs774942476
1000 genomesrs774942476
hgdprs774942476
ensemblrs774942476
gopubmedrs774942476
geneviewrs774942476
scholarrs774942476
googlers774942476
pharmgkbrs774942476
gwascentralrs774942476
openSNPrs774942476
23andMers774942476
23andMe allrs774942476
SNP Nexus

SNPshotrs774942476
SNPdbers774942476
MSV3drs774942476
GWAS Ctlgrs774942476
Max Magnitude0
ClinVar
Risk rs774942476(A;A)
Alt rs774942476(A;A)
Reference rs774942476(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.32994067G>A
CLNSRC
CLNACC RCV000183747.1,