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: rs1057519201
rs1057519201
2 1.000 15 26621395 missense variant T/C snv 0.700 1.000 1 2017 2017
dbSNP: rs12185644
rs12185644
1 1.000 2 57824634 intergenic variant C/A snv 0.66 0.700 1.000 1 2018 2018
dbSNP: rs13020210
rs13020210
1 1.000 2 144623658 intergenic variant G/A snv 0.73 0.700 1.000 1 2018 2018
dbSNP: rs797045045
rs797045045
2 1.000 15 26567721 missense variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs1567106381
rs1567106381
2 1.000 15 26561117 missense variant T/G snv 0.700 0