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rs774663443

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs774663443(C;T)
Make rs774663443(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32878511
GenePKP2
is asnp
is mentioned by
dbSNPrs774663443
ebirs774663443
HLIrs774663443
Exacrs774663443
Varsomers774663443
Maprs774663443
PheGenIrs774663443
hapmaprs774663443
1000 genomesrs774663443
hgdprs774663443
ensemblrs774663443
gopubmedrs774663443
geneviewrs774663443
scholarrs774663443
googlers774663443
pharmgkbrs774663443
gwascentralrs774663443
openSNPrs774663443
23andMers774663443
23andMe allrs774663443
SNP Nexus

SNPshotrs774663443
SNPdbers774663443
MSV3drs774663443
GWAS Ctlgrs774663443
Max Magnitude0
ClinVar
Risk rs774663443(T;T)
Alt rs774663443(T;T)
Reference rs774663443(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.33031445C>T
CLNSRC
CLNACC RCV000183724.1,