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: rs3764650
rs3764650
0.790 0.200 19 1046521 intron variant T/G snv 0.14
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
Mental Disorders 0.010 1.000 1 2019 2019