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: rs17293632
rs17293632
8 0.763 0.240 15 67150258 intron variant C/T snv 0.17 0.700 1.000 3 2015 2017
dbSNP: rs35874463
rs35874463
7 0.827 0.120 15 67165360 missense variant A/G snv 4.0E-02 3.4E-02 0.700 1.000 1 2016 2016
dbSNP: rs72743477
rs72743477
14 0.724 0.240 15 67171953 intron variant A/G snv 0.17 0.700 1.000 1 2015 2015