Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6557013
LINC02234
1.000 0.040 5 97871838 intron variant T/A snv 0.97 1
rs4140564 1.000 0.040 1 186755871 intergenic variant G/A snv 0.93 1
rs226794
ADAMTS5
0.882 0.160 21 26930036 missense variant A/G snv 0.83 0.89 3
rs10795550
ITIH5
1.000 0.040 10 7562392 3 prime UTR variant T/C;G snv 0.88 1
rs6746030
SCN1A-AS1 ; SCN9A
0.763 0.320 2 166242648 missense variant A/G snv 0.88 0.88 16
rs1998094
LINC02319
1.000 0.040 14 52116741 intron variant C/T snv 0.86 1
rs912428
LRCH1
0.925 0.040 13 46593768 intron variant A/G snv 0.84 2
rs1034762
COL2A1
1.000 0.040 12 47995860 intron variant A/C snv 0.74 0.79 1
rs2979715
STMN2
1.000 0.040 8 79650024 intron variant C/T snv 0.77 1
rs317630
CPSF6
1.000 0.040 12 69244067 intron variant T/C snv 0.76 1
rs1627411 1.000 0.040 14 42702125 intron variant T/C snv 0.75 1
rs643472 0.925 0.080 8 29296260 intergenic variant C/T snv 0.73 2
rs1800797
IL6 ; IL6-AS1 ; STEAP1B
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1052981
SFRP4 ; EPDR1
1.000 0.040 7 37906899 3 prime UTR variant G/A snv 0.70 1
rs1566347
SORBS2
1.000 0.040 4 185811412 intron variant T/C snv 0.69 1
rs2966417
LOC105375451
1.000 0.040 7 110517489 intron variant A/G snv 0.69 1
rs4931462 1.000 0.040 12 31225008 TF binding site variant T/G snv 0.65 1
rs614332 1.000 0.040 11 93101032 intergenic variant C/T snv 0.62 1
rs2073711
CILP
0.807 0.160 15 65201874 missense variant A/G snv 0.56 0.61 7
rs3771501
TGFA
0.925 0.040 2 70490521 intron variant A/G snv 0.60 2
rs2862851
TGFA
1.000 0.040 2 70485670 intron variant T/C snv 0.58 1
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs679620
MMP3
0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 17
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47