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: rs386833627
rs386833627
1 1.000 0.120 1 40097122 missense variant A/T snv 0.800 1.000 7 1995 2012
dbSNP: rs386833642
rs386833642
1 1.000 0.120 1 40092082 missense variant A/C snv 4.0E-06 7.0E-06 0.800 1.000 7 1995 2012
dbSNP: rs386833646
rs386833646
1 1.000 0.120 1 40091349 missense variant G/A snv 2.0E-05 4.9E-05 0.700 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: rs386833658
rs386833658
1 1.000 0.120 1 40080458 missense variant G/A;C snv 4.0E-06 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: rs386833665
rs386833665
1 1.000 0.120 1 40076901 missense variant A/G snv 8.0E-06 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: 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: rs1057516447
rs1057516447
1 1.000 0.120 1 40092080 stop gained G/T snv 0.700 0
dbSNP: rs1057516889
rs1057516889
1 1.000 0.120 1 40078632 frameshift variant -/T delins 4.0E-06 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
dbSNP: rs1057517192
rs1057517192
1 1.000 0.120 1 40092448 frameshift variant T/- delins 0.700 0
dbSNP: rs1057517368
rs1057517368
1 1.000 0.120 1 40097113 splice donor variant A/T snv 0.700 0
dbSNP: rs1057517401
rs1057517401
1 1.000 0.120 1 40092044 splice donor variant C/T snv 0.700 0
dbSNP: rs1553166135
rs1553166135
1 1.000 0.120 1 40074147 stop gained G/A snv 0.700 0
dbSNP: rs1553166147
rs1553166147
1 1.000 0.120 1 40074185 splice acceptor variant T/C snv 0.700 0
dbSNP: rs1553166499
rs1553166499
1 1.000 0.120 1 40078565 frameshift variant A/- delins 0.700 0
dbSNP: rs1553167415
rs1553167415
1 1.000 0.120 1 40091328 splice donor variant C/T snv 0.700 0
dbSNP: rs1553167430
rs1553167430
1 1.000 0.120 1 40091401 splice acceptor variant T/C snv 0.700 0