rs369698072, NBAS

N. diseases: 2
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.
SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY
CUI: C3541319
Disease: SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY
4 0.925 0.040 2 15238670 missense variant C/A;T snv 2.8E-05 0.820 1.000 2 2010 2017
Liver Failure, Acute
CUI: C0162557
Disease: Liver Failure, Acute
21 0.925 0.040 2 15238670 missense variant C/A;T snv 2.8E-05 0.010 1.000 1 2017 2017