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rs794729109

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794729109(A;T)
Make rs794729109(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32824047
GenePKP2
is asnp
is mentioned by
dbSNPrs794729109
ebirs794729109
HLIrs794729109
Exacrs794729109
Varsomers794729109
Maprs794729109
PheGenIrs794729109
hapmaprs794729109
1000 genomesrs794729109
hgdprs794729109
ensemblrs794729109
gopubmedrs794729109
geneviewrs794729109
scholarrs794729109
googlers794729109
pharmgkbrs794729109
gwascentralrs794729109
openSNPrs794729109
23andMers794729109
23andMe allrs794729109
SNP Nexus

SNPshotrs794729109
SNPdbers794729109
MSV3drs794729109
GWAS Ctlgrs794729109
Max Magnitude0
ClinVar
Risk rs794729109(T;T)
Alt rs794729109(T;T)
Reference rs794729109(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.32976981T>A
CLNSRC
CLNACC RCV000183756.1,