Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2388334
rs2388334 		0.882 0.040 6 98143746 intron variant A/G snv 0.39
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2019 2019
dbSNP: rs2388334
rs2388334 		0.882 0.040 6 98143746 intron variant A/G snv 0.39
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		0.700 1.000 1 2019 2019
dbSNP: rs2388334
rs2388334 		0.882 0.040 6 98143746 intron variant A/G snv 0.39
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders 		0.700 1.000 1 2019 2019
dbSNP: rs2388334
rs2388334 		0.882 0.040 6 98143746 intron variant A/G snv 0.39
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs2388334
rs2388334 		0.882 0.040 6 98143746 intron variant A/G snv 0.39
CUI: C0236773
Disease: Depressed bipolar I disorder
Depressed bipolar I disorder 		0.700 1.000 1 2019 2019