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: rs10769966
rs10769966
1 11 8825494 intron variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10840133
rs10840133
1 11 8824822 intron variant G/A snv 0.44 0.700 1.000 1 2016 2016
dbSNP: rs35762459
rs35762459
1 11 8823106 intron variant -/A delins 0.46 0.700 1.000 1 2016 2016