Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 16
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30 15
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 14
rs1057523354
COL4A1
0.763 0.480 13 110179387 missense variant C/A snv 13
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs2855812
MICB
0.790 0.360 6 31504943 intron variant G/T snv 0.23 13
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 12
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 12
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 12
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 12
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 12
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 12
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 11
rs3830041
NOTCH4
0.752 0.280 6 32223562 intron variant C/T snv 0.11 11
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 11
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 11
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 10
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11 10
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 10
rs1480380
HLA-DMB
0.763 0.360 6 32945469 intron variant C/T snv 0.11 10
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs185819
TNXB
0.851 0.200 6 32082290 missense variant T/A;C;G snv 8.2E-06; 0.58; 4.1E-06 10
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 10
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 10
rs389884
STK19 ; CYP21A2 ; DXO
0.776 0.440 6 31973120 non coding transcript exon variant A/G snv 7.1E-02 10