Source: ALL

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: rs144660248
rs144660248
1.000 0.040 6 32583926 intron variant G/T snv
Child Development Disorders, Pervasive
0.700 1.000 1 2017 2017
dbSNP: rs144660248
rs144660248
1.000 0.040 6 32583926 intron variant G/T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 1.000 1 2017 2017