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: rs112197434
rs112197434
1 4 75932965 intron variant A/T snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs2292533
rs2292533
1 4 75940706 intron variant C/T snv 0.33 0.34 0.700 1.000 1 2018 2018
dbSNP: rs58317633
rs58317633
1 4 75923290 intron variant T/C snv 0.25 0.700 1.000 1 2018 2018
dbSNP: rs72651379
rs72651379
1 4 75927801 intron variant A/G snv 0.12 0.700 1.000 1 2018 2018
dbSNP: rs78105394
rs78105394
1 4 75910805 downstream gene variant A/G snv 9.5E-02 0.700 1.000 1 2018 2018
dbSNP: rs9996608
rs9996608
1 4 75927078 intron variant C/T snv 0.29 0.700 1.000 1 2018 2018