rs104893895, MSX2

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.
CRANIOSYNOSTOSIS, TYPE 2
CUI: C1858160
Disease: CRANIOSYNOSTOSIS, TYPE 2
1 0.882 0.160 5 174729222 missense variant C/A;T snv 0.840 1.000 7 1993 2013
PARIETAL FORAMINA
CUI: C1868598
Disease: PARIETAL FORAMINA
5 0.882 0.160 5 174729222 missense variant C/A;T snv 0.700 0
Craniosynostosis
CUI: C0010278
Disease: Craniosynostosis
90 0.882 0.160 5 174729222 missense variant C/A;T snv 0.010 1.000 1 1996 1996