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: rs2428548
rs2428548
1 11 62543990 intron variant A/G snv 0.31 0.700 1.000 1 2019 2019
dbSNP: rs2428549
rs2428549
1 11 62544922 intron variant A/G snv 0.32 0.700 1.000 1 2018 2018
dbSNP: rs2509967
rs2509967
1 11 62545314 intron variant C/A;G;T snv 0.700 1.000 1 2019 2019