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: rs1567518954
rs1567518954
1 1.000 0.120 16 86072089 regulatory region variant -/TGTCGCCACTGCTATGATTAAAGCTGGGGAAGCTGGACTT delins 0.700 0
dbSNP: rs200661329
rs200661329
48 0.708 0.440 16 576255 splice donor variant G/A;C snv 5.7E-05 0.700 0
dbSNP: rs778139192
rs778139192
14 0.776 0.360 15 89629561 stop gained G/A;T snv 4.1E-06; 7.3E-05 0.700 0
dbSNP: rs869025222
rs869025222
9 0.827 0.240 3 25580574 missense variant T/C snv 0.700 0
dbSNP: rs587777710
rs587777710
8 0.807 0.160 18 22171856 stop gained G/T snv 0.010 1.000 1 2014 2014