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: rs6031431
rs6031431
4 20 44166512 intron variant A/G snv 0.46 0.700 1.000 3 2018 2019
dbSNP: rs6017281
rs6017281
1 20 44175386 intron variant A/G snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs6031435
rs6031435
1 20 44168718 intron variant A/G snv 0.46 0.700 1.000 1 2017 2017