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: rs2155076
rs2155076
1 11 90656697 intron variant C/T snv 0.30 0.700 1.000 2 2018 2019
dbSNP: rs10734135
rs10734135
1 11 90739807 intron variant C/A snv 0.44 0.700 1.000 1 2019 2019
dbSNP: rs1632631
rs1632631
1 11 90697654 intron variant A/G snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs1783803
rs1783803
1 11 90719202 intron variant T/A snv 0.68 0.700 1.000 1 2017 2017
dbSNP: rs4589258
rs4589258
1 11 90738066 intron variant T/A snv 0.68 0.700 1.000 1 2019 2019
dbSNP: rs7926906
rs7926906
1 11 90791122 intron variant C/A;T snv 0.700 1.000 1 2019 2019