Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs2904880
CD19 ; RABEP2
1.000 0.040 16 28933075 missense variant C/G snv 0.72 0.76 2
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 4
rs3894194
GSDMA
0.882 0.120 17 39965740 missense variant G/A snv 0.46 0.41 2
rs443198
NOTCH4
0.851 0.200 6 32222629 synonymous variant A/G snv 0.38 0.39 2
rs6793295
LRRC34
0.827 0.240 3 169800667 missense variant T/C;G snv 0.37; 1.8E-04 1
rs707939
MSH5-SAPCD1 ; MSH5
0.851 0.200 6 31758911 intron variant C/A snv 0.34 0.26 3
rs2239689
TNXB
0.925 0.120 6 32062507 intron variant G/A snv 0.33 0.25 2
rs3130573
PSORS1C2 ; PSORS1C1
1.000 0.040 6 31138491 non coding transcript exon variant A/C;G snv 8.1E-06; 0.33 1
rs2075800
HSPA1L
0.776 0.440 6 31810169 missense variant C/T snv 0.32 0.25 3
rs2304256
TYK2
0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 3
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 2
rs17266594
BANK1
0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 1
rs1035798
AGER
1.000 0.040 6 32183445 splice region variant G/A snv 0.24 0.19 1
rs1133906
SAMD9L
0.925 0.080 7 93135669 synonymous variant C/T snv 0.22 0.28 1
rs1143679
ITGAM
0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 1
rs7774954
HLA-DQB2
0.925 0.120 6 32756412 3 prime UTR variant C/A;T snv 5.9E-02 2
rs2230926
TNFAIP3
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 1
rs35677470
DNASE1L3
0.807 0.160 3 58197909 missense variant G/A;C snv 4.8E-02; 4.0E-06 1
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 3
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 12
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11 10
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 8
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8