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
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 1
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 31
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 1
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 6
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 4
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 1
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 1
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 4
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 1
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 29
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 1
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 1
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 19
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 9
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 7
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 2
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 1
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 1
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 2
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 12