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: rs386833631
rs386833631
1 1.000 0.120 1 40092507 missense variant C/T snv 0.800 1.000 13 1995 2012
dbSNP: rs137852698
rs137852698
2 0.925 0.120 1 40078630 missense variant A/T snv 0.800 1.000 7 1995 2012
dbSNP: rs137852701
rs137852701
1 1.000 0.120 1 40092085 missense variant C/G snv 0.800 1.000 7 1995 2012
dbSNP: rs137852702
rs137852702
1 1.000 0.120 1 40092498 missense variant C/T snv 0.800 1.000 7 1995 2012
dbSNP: rs386833626
rs386833626
1 1.000 0.120 1 40097125 stop gained C/A;T snv 0.800 1.000 7 1995 2012
dbSNP: rs386833627
rs386833627
1 1.000 0.120 1 40097122 missense variant A/T snv 0.800 1.000 7 1995 2012
dbSNP: rs386833647
rs386833647
1 1.000 0.120 1 40089491 missense variant C/T snv 0.800 1.000 7 1995 2012
dbSNP: rs386833657
rs386833657
1 1.000 0.120 1 40080464 missense variant T/C snv 0.800 1.000 7 1995 2012
dbSNP: rs386833661
rs386833661
1 1.000 0.120 1 40078621 missense variant A/G snv 1.4E-05 0.800 1.000 7 1995 2012
dbSNP: rs386833663
rs386833663
1 1.000 0.120 1 40078603 missense variant A/C snv 0.800 1.000 7 1995 2012
dbSNP: rs386833666
rs386833666
1 1.000 0.120 1 40076891 missense variant C/A;T snv 0.800 1.000 7 1995 2012
dbSNP: rs386833669
rs386833669
1 1.000 0.120 1 40074096 missense variant A/G snv 7.0E-06 0.800 1.000 7 1995 2012
dbSNP: rs386833671
rs386833671
1 1.000 0.120 1 40074068 missense variant A/C;G snv 0.800 1.000 7 1995 2012
dbSNP: rs386833637
rs386833637
1 1.000 0.120 1 40092150 inframe deletion AAG/- delins 1.4E-05 0.700 1.000 5 2000 2007
dbSNP: rs386833645
rs386833645
2 0.925 0.120 1 40097236 start lost C/T snv 1.4E-05 0.700 1.000 4 1989 2007
dbSNP: rs1085307087
rs1085307087
1 1.000 0.120 1 40097238 start lost T/C snv 0.700 1.000 2 1998 1998
dbSNP: rs1349528345
rs1349528345
1 1.000 0.120 1 40076863 frameshift variant -/T delins 7.0E-06 0.700 1.000 2 2000 2013
dbSNP: rs1057516575
rs1057516575
1 1.000 0.120 1 40074160 frameshift variant -/A delins 0.700 1.000 1 2000 2000
dbSNP: rs1553166337
rs1553166337
1 1.000 0.120 1 40076840 splice donor variant A/G snv 0.700 1.000 1 2014 2014
dbSNP: rs386833625
rs386833625
1 1.000 0.120 1 40097125 frameshift variant C/- delins 0.700 1.000 1 2012 2012
dbSNP: rs386833635
rs386833635
1 1.000 0.120 1 40092457 frameshift variant C/- delins 7.0E-06 0.700 1.000 1 2000 2000
dbSNP: rs386833644
rs386833644
1 1.000 0.120 1 40091364 frameshift variant A/- del 0.700 1.000 1 1998 1998
dbSNP: rs1057516447
rs1057516447
1 1.000 0.120 1 40092080 stop gained G/T snv 0.700 0
dbSNP: rs1057517049
rs1057517049
1 1.000 0.120 1 40092109 frameshift variant -/AAGT delins 0.700 0
dbSNP: rs1057517112
rs1057517112
1 1.000 0.120 1 40097185 frameshift variant TCCATGG/- delins 0.700 0