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: rs70993900
rs70993900 		3 0.882 0.080 6 32618381 intergenic variant C/- delins 4.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs9469220
rs9469220 		5 0.827 0.160 6 32690533 TF binding site variant G/A snv 0.53 0.700 1.000 1 2019 2019
dbSNP: rs1800629
rs1800629
TNF
169 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2016 2016