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: rs2076940
rs2076940
1 8 21978509 intron variant A/G snv 9.5E-02 0.700 1.000 1 2017 2017
dbSNP: rs58141407
rs58141407
3 8 21934261 intron variant C/T snv 0.11 0.700 1.000 1 2019 2019
dbSNP: rs727694
rs727694
1 8 21992451 intron variant T/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs80207740
rs80207740
2 8 21922426 intron variant C/G snv 0.12 0.700 1.000 1 2016 2016