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: rs12044963
rs12044963
2 1.000 0.080 1 111849738 intron variant G/T snv 0.10 0.700 1.000 2 2017 2018
dbSNP: rs1443926
rs1443926
1 1.000 0.080 1 111919280 intron variant A/G snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs1545300
rs1545300
1 1.000 0.080 1 111921382 intron variant C/T snv 0.25 0.700 1.000 1 2018 2018