rs142343894, GREM2

N. diseases: 4
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.
TOOTH AGENESIS, SELECTIVE, 9
CUI: C4310638
Disease: TOOTH AGENESIS, SELECTIVE, 9
11 0.851 0.080 1 240493250 missense variant G/C snv 1.7E-03 1.8E-03 0.700 1.000 1 2015 2015
Hypodontia
CUI: C0020608
Disease: Hypodontia
48 0.851 0.080 1 240493250 missense variant G/C snv 1.7E-03 1.8E-03 0.010 1.000 1 2018 2018
Microdontia (disorder)
CUI: C0240340
Disease: Microdontia (disorder)
6 0.851 0.080 1 240493250 missense variant G/C snv 1.7E-03 1.8E-03 0.010 1.000 1 2018 2018
Taurodontism
CUI: C0266039
Disease: Taurodontism
10 0.851 0.080 1 240493250 missense variant G/C snv 1.7E-03 1.8E-03 0.010 1.000 1 2018 2018