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: rs132570
rs132570
2 1.000 0.040 22 39580123 intron variant C/A snv 0.45 0.700 1.000 2 2019 2019
dbSNP: rs5750853
rs5750853
1 22 39580181 intron variant C/T snv 0.36 0.700 1.000 2 2018 2019
dbSNP: rs132575
rs132575
2 1.000 0.040 22 39586716 intron variant A/G snv 0.51 0.700 1.000 1 2017 2017
dbSNP: rs3788556
rs3788556
1 22 39576157 intron variant T/C snv 0.60 0.700 1.000 1 2019 2019
dbSNP: rs3788568
rs3788568
1 22 39615268 intron variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs5750854
rs5750854
1 22 39594770 intron variant C/T snv 0.22 0.700 1.000 1 2019 2019
dbSNP: rs5757730
rs5757730
2 1.000 0.040 22 39571425 intron variant A/G snv 0.55 0.700 1.000 1 2018 2018