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: rs28456
rs28456
5 0.925 0.120 11 61822009 intron variant A/C;G snv 0.710 1.000 1 2018 2018
dbSNP: rs12226877
rs12226877
2 0.925 0.040 11 61824435 intron variant G/A snv 0.14 0.700 1.000 1 2019 2019
dbSNP: rs174576
rs174576
14 0.851 0.200 11 61836038 intron variant C/A;T snv 0.700 1.000 1 2018 2018