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: rs10511071
rs10511071
1 3 85750927 intron variant T/C snv 0.15 0.700 1.000 1 2019 2019
dbSNP: rs1248855
rs1248855
1 3 84970658 intron variant C/T snv 0.11 0.700 1.000 1 2018 2018
dbSNP: rs146282319
rs146282319
1 3 85913541 intron variant C/T snv 3.7E-03 0.700 1.000 1 2018 2018
dbSNP: rs17518584
rs17518584
8 0.827 0.160 3 85555773 intron variant C/T snv 0.50 0.700 1.000 1 2015 2015
dbSNP: rs424029
rs424029
1 3 84960888 intron variant G/A snv 5.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs62253086
rs62253086
1 3 85344665 intron variant T/G snv 0.13 0.700 1.000 1 2018 2018
dbSNP: rs62263923
rs62263923
2 1.000 0.040 3 85625640 intron variant A/G snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs6770622
rs6770622
1 3 85122265 intron variant G/A snv 0.11 0.700 1.000 1 2018 2018
dbSNP: rs73843290
rs73843290
1 3 85096685 intron variant T/C snv 0.11 0.700 1.000 1 2018 2018
dbSNP: rs73845427
rs73845427
1 3 85278368 intron variant G/A snv 3.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs9830359
rs9830359
2 3 85347968 intron variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs9864170
rs9864170
1 3 85561758 intron variant A/G;T snv 0.700 1.000 1 2018 2018