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: rs10197140
rs10197140
3 2 110852366 intron variant T/C snv 0.28 0.700 1.000 1 2016 2016
dbSNP: rs34931195
rs34931195
1 2 111074488 intron variant T/A snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs56088557
rs56088557
1 2 110979246 intron variant A/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs952249
rs952249
1 2 110859574 intron variant G/A snv 0.34 0.700 1.000 1 2019 2019