Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7673984
rs7673984 		1 1.000 0.040 4 54222594 intron variant C/T snv 0.21 0.700 1.000 1 2018 2018
dbSNP: rs7931326
rs7931326
ADAMTS8
1 1.000 0.040 11 130406452 intron variant C/G snv 0.12 0.700 1.000 1 2018 2018
dbSNP: rs9517490
rs9517490
DOCK9
1 1.000 0.040 13 98932051 intron variant T/C snv 0.63 0.700 1.000 1 2018 2018