rs80338827, MYH9

N. diseases: 1
Source: UNIPROT ×
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.
May-Hegglin anomaly
CUI: C0340978
Disease: May-Hegglin anomaly
13 0.882 0.320 22 36305984 missense variant C/T snv 7.0E-06 0.810 1.000 11 2000 2006