Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6746030
SCN1A-AS1 ; SCN9A
0.763 0.320 2 166242648 missense variant A/G snv 0.88 0.88 16
rs226794
ADAMTS5
0.882 0.160 21 26930036 missense variant A/G snv 0.83 0.89 3
rs1676486
COL11A1
0.851 0.120 1 102888582 missense variant A/G;T snv 0.80; 4.0E-06 7
rs1034762
COL2A1
1.000 0.040 12 47995860 intron variant A/C snv 0.74 0.79 1
rs4233367
ADAMTS4
0.925 0.040 1 161193247 missense variant T/A;C snv 0.67 2
rs679620
MMP3
0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 17
rs520540
MMP3
0.925 0.120 11 102838694 synonymous variant A/G snv 0.57 0.54 2
rs602128
MMP3
1.000 0.040 11 102842734 missense variant A/C;G snv 4.0E-06; 0.57 1
rs2073711
CILP
0.807 0.160 15 65201874 missense variant A/G snv 0.56 0.61 7
rs3740199
ADAM12
0.882 0.120 10 126330456 missense variant C/A;G snv 2.1E-03; 0.56 3
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1940475
MMP8
1.000 0.040 11 102722517 missense variant T/C;G snv 0.54 4
rs4343
ACE
0.742 0.480 17 63488670 synonymous variant G/A snv 0.53 14
rs4362
ACE
0.807 0.240 17 63496400 missense variant T/C;G snv 0.52; 1.2E-05 0.51 9
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs352140
TLR9
0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs2908004
WNT16
1.000 0.040 7 121329715 missense variant G/A;T snv 0.44; 4.0E-06 4
rs4586
CCL2
0.790 0.280 17 34256250 synonymous variant T/C snv 0.44 0.48 8
rs4794136
XYLT2
1.000 0.040 17 50356597 synonymous variant T/C snv 0.44 0.47 1
rs4721
LRRC61 ; RARRES2
1.000 0.040 7 150338437 missense variant T/A;C;G snv 0.42 0.47 2
rs225014
DIO2
0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 22
rs1042667
SOX9-AS1 ; SOX9
1.000 0.040 17 72124410 3 prime UTR variant A/C snv 0.41 0.36 3
rs8904
NFKBIA
0.925 0.120 14 35402011 3 prime UTR variant G/A;C;T snv 0.39; 4.0E-06 4
rs2276454
COL2A1 ; LOC105369752
0.925 0.040 12 47982508 synonymous variant G/A snv 0.39 0.38 2
rs11177
SNORD136 ; GNL3 ; SNORD19 ; PBRM1
0.851 0.080 3 52687289 missense variant G/A snv 0.38 0.33 4