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: rs121918110
rs121918110
1 1.000 0.120 10 71819860 missense variant A/G snv 0.800 1.000 2 1991 2007
dbSNP: rs121918105
rs121918105
1 1.000 0.120 10 71819761 missense variant C/A snv 0.700 0
dbSNP: rs121918106
rs121918106
2 0.925 0.120 10 71851221 start lost T/A;C snv 1.3E-05; 6.5E-06 0.700 0
dbSNP: rs121918108
rs121918108
1 1.000 0.120 10 71819762 missense variant A/C snv 0.700 0
dbSNP: rs121918109
rs121918109
1 1.000 0.120 10 71819527 stop gained G/A snv 0.700 0
dbSNP: rs1554879741
rs1554879741
4 0.851 0.120 10 71819093 stop gained C/A snv 0.700 0