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: rs10917477
rs10917477
2 1.000 0.040 1 19534612 intron variant A/C;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs12138950
rs12138950
3 0.925 0.040 1 19512621 intron variant A/C snv 5.4E-03 0.700 1.000 1 2016 2016
dbSNP: rs75491569
rs75491569
1 1.000 0.040 1 19509727 intron variant C/T snv 0.17 0.700 1.000 1 2018 2018