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: rs10191793
rs10191793 		2 106809420 intron variant A/G snv 0.21
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2012 2012
dbSNP: rs1034811
rs1034811 		2 106886868 intron variant C/T snv 0.72
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018