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: rs9488822
rs9488822
FRK
3 6 115991730 intron variant A/T snv 0.35 0.800 1.000 2 2010 2013
dbSNP: rs13210143
rs13210143
FRK
2 6 116068473 intergenic variant G/A snv 0.38 0.700 1.000 1 2019 2019
dbSNP: rs3822857
rs3822857
FRK
3 6 115992768 intron variant G/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs6909746
rs6909746
FRK
1 6 116031587 intron variant C/A;T snv 0.37 0.700 1.000 1 2017 2017
dbSNP: rs72951954
rs72951954
FRK
2 6 116072564 TF binding site variant C/A snv 5.1E-02 0.700 1.000 1 2018 2018