rs104894196, ALX4

N. diseases: 1
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.
PARIETAL FORAMINA 2
CUI: C1865044
Disease: PARIETAL FORAMINA 2
9 1.000 0.120 11 44267585 missense variant C/G;T snv 0.800 1.000 2 2000 2001