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: rs1433850094
rs1433850094
1 1.000 15 60499914 missense variant C/T snv 4.0E-06 0.700 1.000 1 2018 2018
dbSNP: rs1555427497
rs1555427497
1 1.000 15 60531767 missense variant T/C snv 0.700 1.000 1 2018 2018
dbSNP: rs1555427498
rs1555427498
1 1.000 15 60531773 missense variant C/G snv 0.700 1.000 1 2018 2018