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: rs28724212
rs28724212
1.000 0.040 6 32588824 intron variant A/G snv
Child Development Disorders, Pervasive
0.700 1.000 1 2017 2017
dbSNP: rs28724212
rs28724212
1.000 0.040 6 32588824 intron variant A/G snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 1.000 1 2017 2017