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: rs10483205
rs10483205
1 22 40487595 intron variant C/T snv 7.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs17002036
rs17002036
1 22 40601107 intron variant G/A snv 7.8E-02 0.700 1.000 1 2018 2018
dbSNP: rs5995875
rs5995875
1 22 40564688 intron variant C/T snv 9.8E-02 0.700 1.000 1 2016 2016