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rs794729104

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794729104(A;A)
Make rs794729104(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32850896
GenePKP2
is asnp
is mentioned by
dbSNPrs794729104
ebirs794729104
HLIrs794729104
Exacrs794729104
Varsomers794729104
Maprs794729104
PheGenIrs794729104
hapmaprs794729104
1000 genomesrs794729104
hgdprs794729104
ensemblrs794729104
gopubmedrs794729104
geneviewrs794729104
scholarrs794729104
googlers794729104
pharmgkbrs794729104
gwascentralrs794729104
openSNPrs794729104
23andMers794729104
23andMe allrs794729104
SNP Nexus

SNPshotrs794729104
SNPdbers794729104
MSV3drs794729104
GWAS Ctlgrs794729104
Max Magnitude0
ClinVar
Risk rs794729104(A;A)
Alt rs794729104(A;A)
Reference rs794729104(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.33003830A>T
CLNSRC
CLNACC RCV000183738.1,