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: rs10821415
rs10821415
1 1.000 0.080 9 94951177 intron variant C/A snv 0.34 0.810 1.000 3 2012 2018
dbSNP: rs7026071
rs7026071
1 1.000 0.080 9 94730238 intron variant T/A;C snv 0.700 1.000 2 2017 2018
dbSNP: rs4385527
rs4385527
6 0.827 0.280 9 94886305 intron variant G/A snv 0.31 0.700 1.000 1 2018 2018