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: rs2494738
rs2494738
1 1.000 0.080 14 104780349 intron variant G/A snv 1.0E-01 0.010 1.000 1 2017 2017
dbSNP: rs2494746
rs2494746
1 1.000 0.080 14 104791382 intron variant C/G snv 0.77 0.010 1.000 1 2017 2017
dbSNP: rs2498786
rs2498786
2 0.925 0.160 14 104796031 upstream gene variant C/G snv 0.50 0.010 1.000 1 2015 2015
dbSNP: rs3803304
rs3803304
3 0.882 0.160 14 104772809 intron variant C/G snv 0.24 0.010 1.000 1 2017 2017