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: rs41352752
rs41352752
1 5 88733391 intron variant T/C;G snv 0.700 1.000 3 2017 2019
dbSNP: rs61104616
rs61104616
1 5 88867954 intron variant G/A snv 0.47 0.700 1.000 3 2018 2019
dbSNP: rs770463
rs770463
1 5 88899133 intron variant C/T snv 0.61 0.700 1.000 2 2018 2018
dbSNP: rs10514303
rs10514303
2 5 88749212 intron variant C/A;G snv 6.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs1422189
rs1422189
1 5 88746202 intron variant G/A snv 0.10 0.700 1.000 1 2019 2019
dbSNP: rs254779
rs254779
1 5 88723812 intron variant T/C snv 0.46 0.700 1.000 1 2017 2017
dbSNP: rs34316
rs34316
1 5 88719728 3 prime UTR variant A/C snv 0.50 0.700 1.000 1 2018 2018
dbSNP: rs3850651
rs3850651
1 5 88885292 intron variant T/A;C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs62380364
rs62380364
1 5 88811520 intron variant C/A snv 0.36 0.700 1.000 1 2019 2019