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
rs17228212
SMAD3
0.807 0.160 15 67166301 intron variant T/C snv 0.21 8
rs3869109 0.851 0.160 6 31216419 intergenic variant A/G;T snv 5
rs7984870
TNFSF11
0.925 0.160 13 42572346 intron variant G/C snv 0.46 2
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 12
rs12953
PECAM1
0.763 0.200 17 64356203 missense variant C/A;T snv 0.38 9
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs1878406 0.807 0.200 4 147472512 intergenic variant C/A;G;T snv 7
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs17757541
BCL2
0.827 0.240 18 63212453 intron variant C/G;T snv 7
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 10
rs644045
CYP21A2 ; C2
0.851 0.240 6 31916180 intron variant A/G snv 0.72 4
rs9770242
NAMPT
0.851 0.240 7 106285885 5 prime UTR variant C/A snv 0.79 5
rs805297
BAG6 ; APOM
0.851 0.280 6 31654829 intron variant C/A snv 0.23 6
rs112735431
RNF213 ; RNF213-AS1
0.683 0.320 17 80385145 missense variant G/A;C snv 2.6E-04; 8.0E-06 24
rs2072633
CFB ; CYP21A2 ; NELFE
0.807 0.320 6 31951801 3 prime UTR variant A/G snv 0.59 6
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
rs8193037
IL17A
0.752 0.320 6 52186311 upstream gene variant G/A;T snv 12
rs237025
SUMO4 ; TAB2
0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs3027898
IRAK1
0.752 0.360 X 154010439 downstream gene variant C/A snv 11
rs4711998
IL17A
0.708 0.360 6 52185555 upstream gene variant A/G snv 0.64 16
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27