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: rs1530440
rs1530440
6 1.000 0.040 10 61764833 intron variant C/T snv 0.15 0.700 1.000 3 2009 2018
dbSNP: rs4590817
rs4590817
5 10 61707795 intron variant G/C snv 0.15 0.700 1.000 2 2017 2018
dbSNP: rs72831345
rs72831345
4 10 61758990 intron variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs7922049
rs7922049
3 10 61702607 intron variant G/A;C snv 0.700 1.000 1 2018 2018