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: rs10088255
rs10088255 		8 102355371 intron variant A/T snv 0.55
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs4734619
rs4734619 		8 102377272 intron variant C/G snv 0.77
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs7827839
rs7827839 		8 102341502 intron variant C/T snv 0.59
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs7840202
rs7840202 		0.851 0.160 8 102296172 intron variant A/C snv 0.21
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		Mental Disorders 0.700 1.000 1 2011 2011
dbSNP: rs7840202
rs7840202 		0.851 0.160 8 102296172 intron variant A/C snv 0.21
CUI: C1270972
Disease: Mild cognitive disorder
Mild cognitive disorder 		Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs7840202
rs7840202 		0.851 0.160 8 102296172 intron variant A/C snv 0.21
CUI: C0039373
Disease: Tay-Sachs Disease
Tay-Sachs Disease 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs7840202
rs7840202 		0.851 0.160 8 102296172 intron variant A/C snv 0.21
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.010 1.000 1 2011 2011