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rs587777534

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777534(C;T)
Make rs587777534(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position88296207
GeneCTSC
is asnp
is mentioned by
dbSNPrs587777534
ebirs587777534
HLIrs587777534
Exacrs587777534
Varsomers587777534
Maprs587777534
PheGenIrs587777534
hapmaprs587777534
1000 genomesrs587777534
hgdprs587777534
ensemblrs587777534
gopubmedrs587777534
geneviewrs587777534
scholarrs587777534
googlers587777534
pharmgkbrs587777534
gwascentralrs587777534
openSNPrs587777534
23andMers587777534
23andMe allrs587777534
SNP Nexus

SNPshotrs587777534
SNPdbers587777534
MSV3drs587777534
GWAS Ctlgrs587777534
Max Magnitude0
ClinVar
Risk rs587777534(G,T;G,T)
Alt rs587777534(G,T;G,T)
Reference rs587777534(C;C)
Significance Pathogenic
Disease Periodontitis
Variation info
Gene CTSC
CLNDBN Periodontitis, aggressive, 1
Reversed 0
HGVS NC_000011.9:g.88029375C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000128620.3,