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: rs2929508
rs2929508
1 15 71954623 intron variant A/T snv 0.55 0.700 1.000 1 2019 2019
dbSNP: rs2957740
rs2957740
1 15 72015350 intron variant A/G snv 0.64 0.700 1.000 1 2019 2019
dbSNP: rs2957742
rs2957742
1 15 72010553 intron variant G/A;C snv 0.700 1.000 1 2019 2019