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: rs1275988
rs1275988
6 1.000 0.080 2 26691496 upstream gene variant C/T snv 0.48 0.700 1.000 4 2017 2018
dbSNP: rs2586886
rs2586886
4 1.000 0.080 2 26709163 intron variant C/G;T snv 0.700 1.000 3 2016 2019
dbSNP: rs35021474
rs35021474
4 2 26693976 intron variant C/G snv 0.48 0.700 1.000 2 2018 2018
dbSNP: rs1275982
rs1275982
3 2 26696221 intron variant C/T snv 0.48 0.700 1.000 1 2018 2018
dbSNP: rs1731243
rs1731243
4 2 26707543 intron variant C/T snv 0.48 0.700 1.000 1 2018 2018
dbSNP: rs1731249
rs1731249
5 2 26697157 intron variant T/A snv 0.48 0.700 1.000 1 2018 2018