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rs28937571

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0
Make rs28937571(A;G)
Make rs28937571(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position88294163
GeneCTSC
is asnp
is mentioned by
dbSNPrs28937571
ClinGenrs28937571
ebirs28937571
HLIrs28937571
Exacrs28937571
Varsomers28937571
Maprs28937571
PheGenIrs28937571
hapmaprs28937571
1000 genomesrs28937571
hgdprs28937571
ensemblrs28937571
gopubmedrs28937571
geneviewrs28937571
scholarrs28937571
googlers28937571
pharmgkbrs28937571
gwascentralrs28937571
openSNPrs28937571
23andMers28937571
23andMe allrs28937571
SNP Nexus

SNPshotrs28937571
SNPdbers28937571
MSV3drs28937571
GWAS Ctlgrs28937571
Max Magnitude0
OMIM602365
DescPERIODONTITIS, AGGRESSIVE, 1
Variant0012
Relatedalso


ClinVar
Risk rs28937571(G;G)
Alt rs28937571(G;G)
Reference Rs28937571(A;A)
Significance Pathogenic
Disease Periodontitis
Variation info
Gene CTSC
CLNDBN Periodontitis, aggressive, 1
Reversed 1
HGVS NC_000011.9:g.88027331T>C
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000007723.3,