Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10817938 0.882 0.080 9 97700127 non coding transcript exon variant T/C snv 3.2E-02 5
rs10818524
GSN
1.000 0.040 9 121267901 intron variant T/C snv 0.37 1
rs10971638 1.000 0.040 9 33674679 non coding transcript exon variant C/T snv 0.21 1
rs11134527 0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs1126809 0.683 0.320 11 89284793 missense variant G/A snv 0.18 0.18 29
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs115169993 1.000 0.040 1 162772032 missense variant G/A snv 7.8E-04 2.9E-03 1
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11549467 0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs116150891 1.000 0.040 9 21970929 missense variant G/A;C snv 5.6E-04 2.6E-03 1
rs11707807
LPP
1.000 0.040 3 188370473 intron variant A/G snv 0.36 1
rs117984432 1.000 0.040 16 89388583 intron variant T/C snv 2.0E-02 1
rs1194611372 0.763 0.320 1 152032679 missense variant A/C snv 9
rs12108497 0.851 0.080 4 184650403 intron variant C/G;T snv 6
rs121434568 0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614