rs757863670, B9D2

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.
Familial aplasia of the vermis
CUI: C0431399
Disease: Familial aplasia of the vermis
187 0.925 0.160 19 41358004 missense variant A/G snv 1.2E-05 0.700 1.000 1 2015 2015
MECKEL SYNDROME, TYPE 10
CUI: C3280036
Disease: MECKEL SYNDROME, TYPE 10
4 0.925 0.160 19 41358004 missense variant A/G snv 1.2E-05 0.700 1.000 1 2015 2015