INHA, inhibin subunit alpha, 3623

N. diseases: 91; N. variants: 5
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: rs11893842
rs11893842
0.925 0.160 2 219572251 intron variant A/G snv 0.45
CUI: C0175754
Disease: Agenesis of corpus callosum
Agenesis of corpus callosum
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases 0.010 1.000 1 2014 2014