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rs78897684

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs78897684(A;A)
Make rs78897684(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32824163
GenePKP2
is asnp
is mentioned by
dbSNPrs78897684
ebirs78897684
HLIrs78897684
Exacrs78897684
Varsomers78897684
Maprs78897684
PheGenIrs78897684
hapmaprs78897684
1000 genomesrs78897684
hgdprs78897684
ensemblrs78897684
gopubmedrs78897684
geneviewrs78897684
scholarrs78897684
googlers78897684
pharmgkbrs78897684
gwascentralrs78897684
openSNPrs78897684
23andMers78897684
23andMe allrs78897684
SNP Nexus

SNPshotrs78897684
SNPdbers78897684
MSV3drs78897684
GWAS Ctlgrs78897684
Max Magnitude0
ClinVar
Risk rs78897684(G;G)
Alt rs78897684(G;G)
Reference rs78897684(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.32977097C>G
CLNSRC
CLNACC RCV000183751.2,