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: rs10953024
rs10953024
2 7 90874752 intron variant T/C snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs12674916
rs12674916
1 8 142876542 intron variant G/A snv 0.52 0.700 1.000 1 2019 2019
dbSNP: rs34346910
rs34346910
1 10 86667452 upstream gene variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs57712673
rs57712673
1 19 14774988 intron variant T/A snv 0.31 0.700 1.000 1 2017 2017
dbSNP: rs5895733
rs5895733
1 8 142878062 intron variant AT/- del 0.59 0.700 1.000 1 2019 2019
dbSNP: rs59964204
rs59964204
1 7 36899717 intron variant G/A snv 0.32 0.700 1.000 1 2017 2017
dbSNP: rs6988985
rs6988985
1 8 142925688 intergenic variant T/C snv 0.60 0.700 1.000 1 2017 2017
dbSNP: rs7075481
rs7075481
1 10 8346355 intergenic variant A/G snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs9692804
rs9692804
1 8 142977208 downstream gene variant G/A snv 0.38 0.700 1.000 1 2019 2019