Disease: Rheumatoid Arthritis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10774624
LINC02356
0.882 0.160 12 111395984 intron variant G/A snv 0.67 6
rs10903323
MSRA
0.807 0.160 8 10292057 intron variant A/G snv 0.15 8
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 12
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs17228212
SMAD3
0.807 0.160 15 67166301 intron variant T/C snv 0.21 8
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs17757541
BCL2
0.827 0.240 18 63212453 intron variant C/G;T snv 7
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2069705
IFNG-AS1 ; IFNG
0.695 0.440 12 68161231 intron variant G/A;C snv 19
rs2237892
KCNQ1
0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 16
rs2243115
IL12A-AS1 ; IL12A
0.776 0.320 3 159988493 intron variant T/G snv 0.10 12
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs2430561
IFNG ; IFNG-AS1
0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs3819025
IL17A
0.752 0.480 6 52186476 intron variant G/A snv 0.13 8.5E-02 11
rs644045
CYP21A2 ; C2
0.851 0.240 6 31916180 intron variant A/G snv 0.72 4
rs7044343
LOC107987046 ; IL33
0.752 0.520 9 6254208 intron variant C/T snv 0.51 13
rs755622
MIF-AS1 ; MIF
0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs7984870
TNFSF11
0.925 0.160 13 42572346 intron variant G/C snv 0.46 2
rs805297
BAG6 ; APOM
0.851 0.280 6 31654829 intron variant C/A snv 0.23 6
rs1878406 0.807 0.200 4 147472512 intergenic variant C/A;G;T snv 7