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rs762103704

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs762103704(A;T)
Make rs762103704(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32850764
GenePKP2
is asnp
is mentioned by
dbSNPrs762103704
ebirs762103704
HLIrs762103704
Exacrs762103704
Varsomers762103704
Maprs762103704
PheGenIrs762103704
hapmaprs762103704
1000 genomesrs762103704
hgdprs762103704
ensemblrs762103704
gopubmedrs762103704
geneviewrs762103704
scholarrs762103704
googlers762103704
pharmgkbrs762103704
gwascentralrs762103704
openSNPrs762103704
23andMers762103704
23andMe allrs762103704
SNP Nexus

SNPshotrs762103704
SNPdbers762103704
MSV3drs762103704
GWAS Ctlgrs762103704
Max Magnitude0
ClinVar
Risk rs762103704(T;T)
Alt rs762103704(T;T)
Reference rs762103704(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.33003698A>T
CLNSRC
CLNACC RCV000183743.1,