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: rs17567417
rs17567417
2 1.000 0.040 2 33205536 intron variant G/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2061026
rs2061026
1 1.000 0.040 2 33210282 intron variant A/G snv 0.52 0.700 1.000 1 2018 2018
dbSNP: rs4630744
rs4630744
2 0.925 0.040 2 33236308 intron variant A/G snv 0.39 0.700 1.000 1 2019 2019