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: rs1331463984
rs1331463984
33 0.701 0.240 16 2176350 missense variant G/A snv 0.800 0
dbSNP: rs1567252467
rs1567252467
1 1.000 16 2173504 missense variant A/G snv 0.700 0
dbSNP: rs1567252659
rs1567252659
1 1.000 16 2173812 missense variant C/G;T snv 0.700 0
dbSNP: rs1567254067
rs1567254067
1 1.000 16 2176103 missense variant A/G snv 0.700 0