rs140981580, SSUH2

N. diseases: 1
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Dentin dysplasia, type 1
CUI: C0399379
Disease: Dentin dysplasia, type 1
2 1.000 0.080 3 8630911 missense variant G/A;T snv 6.1E-05; 2.9E-04 0.010 1.000 1 2017 2017