Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 34
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 31
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 4
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 3
rs886040971 0.683 0.280 8 115604339 stop gained G/A;T snv 56
rs113871094 0.683 0.320 15 48465820 stop gained G/A snv 34
rs80338945 0.695 0.440 13 20189313 missense variant A/G snv 6.4E-04 6.4E-04 32
rs398124401 0.695 0.480 4 55346393 stop gained G/A snv 1.2E-04 2.8E-05 25
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 7
rs1331463984 0.701 0.240 16 2176350 missense variant G/A snv 33
rs765379963 0.701 0.520 1 165743172 stop gained G/A snv 1.2E-05 2.1E-05 19
rs1344706 0.701 0.160 2 184913701 intron variant A/C;T snv 1
rs1563183492 0.708 0.520 7 70766248 missense variant C/T snv 32
rs1085307993 0.716 0.440 5 161331056 missense variant C/T snv 53
rs148881970 0.724 0.360 17 42543840 missense variant A/G snv 5.4E-05 1.3E-04 22
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 1
rs555145190 0.732 0.360 17 42543921 stop gained G/A;C;T snv 4.2E-06 21
rs587784105 0.732 0.440 5 177235863 stop gained G/A snv 19
rs28935468 0.732 0.240 X 154030912 missense variant G/A snv 14
rs1057518345 0.742 0.400 20 50894172 frameshift variant ACTA/- delins 25
rs1562127631 0.742 0.360 6 78961751 frameshift variant C/- del 24
rs1566823361 0.742 0.440 13 101726732 frameshift variant -/G delins 18
rs113994098 0.742 0.320 15 89321792 missense variant C/T snv 1.5E-04 2.7E-04 10
rs4343
ACE
0.742 0.480 17 63488670 synonymous variant G/A snv 0.53 1