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: rs770463
rs770463
1 5 88899133 intron variant C/T snv 0.61 0.700 1.000 2 2018 2018
dbSNP: rs304132
rs304132
1 5 88919777 intron variant A/G snv 0.67 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: rs62378245
rs62378245
3 1.000 0.040 5 89448145 intron variant C/T snv 0.25 0.700 1.000 1 2019 2019