rs28934608, F11

N. diseases: 3
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.
Hereditary Factor XI Deficiency
CUI: C0015523
Disease: Hereditary Factor XI Deficiency
119 0.925 0.160 4 186280333 missense variant C/T snv 2.4E-05 2.1E-05 0.800 1.000 21 1989 2019
Androgenetic Alopecia
CUI: C0162311
Disease: Androgenetic Alopecia
107 0.925 0.160 4 186280333 missense variant C/T snv 2.4E-05 2.1E-05 0.010 1.000 1 1999 1999
Gestational Trophoblastic Neoplasms
CUI: C1135868
Disease: Gestational Trophoblastic Neoplasms
7 0.925 0.160 4 186280333 missense variant C/T snv 2.4E-05 2.1E-05 0.010 1.000 1 1999 1999