Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1418810723
FN1
0.851 0.080 2 215409981 missense variant A/T snv 8.0E-06 9
rs1443465532 0.882 0.080 6 43774362 missense variant G/C snv 4.0E-06 7.0E-06 6
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs17217772 0.790 0.240 2 47410107 missense variant A/C;G;T snv 5.8E-03 10
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs200863613 0.925 0.080 9 21971061 missense variant C/A;T snv 8.5E-05 3.7E-04 6
rs201216664 0.851 0.080 17 51171503 missense variant A/G snv 5
rs2016347 0.790 0.160 15 98960571 3 prime UTR variant G/A;T snv 9
rs2057482 0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
rs2073778 22 20087052 non coding transcript exon variant C/T snv 0.12 1
rs2227983 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 31
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs3136797 0.827 0.120 8 42369287 missense variant C/G snv 1.1E-02 1.1E-02 10
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs367597251 0.807 0.080 12 68839587 missense variant A/G snv 1.5E-04 5.1E-04 10
rs375874539 0.732 0.320 17 7674237 missense variant G/A;C snv 15
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs438034 0.882 0.120 1 214657274 stop gained A/G;T snv 0.61 4
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 23
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131