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: rs9469003
rs9469003
LINC01149
6 0.882 0.160 6 31440051 intron variant T/C snv 0.22 0.700 1.000 1 2011 2011
dbSNP: rs9888871
rs9888871 		2 0.925 0.160 16 49916730 downstream gene variant G/C snv 0.19 0.700 1.000 1 2017 2017
dbSNP: rs9933632
rs9933632 		3 0.882 0.240 16 49906847 intergenic variant G/T snv 0.31 0.010 1.000 1 2018 2018
dbSNP: rs3834129
rs3834129
CASP8
38 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 0.010 1.000 1 2017 2017