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: rs62408225
rs62408225
2 1.000 0.120 6 90246690 intron variant A/G snv 0.26 0.700 1.000 2 2016 2019
dbSNP: rs17585295
rs17585295
2 6 90235112 intron variant C/T snv 0.27 0.700 1.000 1 2016 2016
dbSNP: rs182491379
rs182491379
1 6 90129545 intron variant C/T snv 4.3E-03 0.700 1.000 1 2019 2019
dbSNP: rs72923978
rs72923978
1 6 90028558 intron variant C/G;T snv 9.0E-02 0.700 1.000 1 2019 2019