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rs749926313

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs749926313(G;G)
Make rs749926313(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32841169
GenePKP2
is asnp
is mentioned by
dbSNPrs749926313
ebirs749926313
HLIrs749926313
Exacrs749926313
Varsomers749926313
Maprs749926313
PheGenIrs749926313
hapmaprs749926313
1000 genomesrs749926313
hgdprs749926313
ensemblrs749926313
gopubmedrs749926313
geneviewrs749926313
scholarrs749926313
googlers749926313
pharmgkbrs749926313
gwascentralrs749926313
openSNPrs749926313
23andMers749926313
23andMe allrs749926313
SNP Nexus

SNPshotrs749926313
SNPdbers749926313
MSV3drs749926313
GWAS Ctlgrs749926313
Max Magnitude0
ClinVar
Risk rs749926313(C;C)
Alt rs749926313(C;C)
Reference rs749926313(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.32994103T>C
CLNSRC
CLNACC RCV000183744.1,