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: rs1316615934
rs1316615934
2 0.925 15 82151809 missense variant A/T snv 8.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs1441937959
rs1441937959
20 0.763 0.280 15 82240555 missense variant T/C snv 8.2E-06 0.010 1.000 1 2019 2019
dbSNP: rs376095522
rs376095522
1 1.000 15 82130452 missense variant C/T snv 2.8E-05 3.5E-05 0.010 1.000 1 2019 2019