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: rs10910937
rs10910937
1 181428088 intron variant T/C snv 0.11
CUI: C0002418
Disease: Amblyopia
Amblyopia
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases 0.700 1.000 1 2018 2018