Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12666409
DDC
1.000 0.080 7 50567279 upstream gene variant T/A snv 0.21 1
rs74501188 1.000 0.080 5 90931162 5 prime UTR variant G/A snv 0.17 1
rs717620 0.763 0.240 10 99782821 5 prime UTR variant C/T snv 0.17 0.15 10
rs3124599 0.851 0.080 9 136509318 intron variant G/A snv 0.13 5
rs4760 1.000 0.080 19 43648948 missense variant A/G snv 0.12 0.11 8
rs1045494 0.882 0.120 2 201287058 3 prime UTR variant T/C snv 0.10 3
rs12200782 1.000 0.080 6 26402808 intron variant C/G snv 7.9E-02 1
rs141670911 1.000 0.080 6 26581030 intergenic variant A/T snv 7.3E-02 1
rs4324798 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 8
rs17185553 1.000 0.080 9 17934122 intron variant G/C snv 6.5E-02 1
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs4866 0.827 0.240 7 2249951 missense variant G/A snv 2.2E-02 1.8E-02 5
rs140013431 1.000 0.080 6 7770278 intron variant T/C snv 1.2E-02 1
rs56391007
MET
0.752 0.200 7 116771936 missense variant C/T snv 7.9E-03 9.0E-03 16
rs141877527 1.000 0.080 10 33497992 intergenic variant A/G snv 7.3E-03 1
rs117729306 1.000 0.080 11 8465623 non coding transcript exon variant T/C snv 7.3E-03 1
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs34589476
MET
0.827 0.160 7 116771869 missense variant C/T snv 2.9E-03 3.2E-03 7
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs1429133479 1.000 0.080 22 25847461 missense variant G/A snv 1.4E-05 1
rs148924904 0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06 17
rs577715207 0.827 0.160 3 189886413 missense variant T/A;C snv 4.0E-06; 4.0E-06 7.0E-06 8
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134