MSX2, msh homeobox 2, 4488

N. diseases: 135; N. variants: 7
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs104893895
rs104893895
0.882 0.160 5 174729222 missense variant C/A;T snv
CUI: C1868598
Disease: PARIETAL FORAMINA
PARIETAL FORAMINA
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases 0.700 0