Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs974819 0.807 0.080 11 103789839 intron variant T/A;C snv 2
rs17398575 0.882 0.040 7 106769006 intron variant G/A snv 0.20 1
rs6601530
PINX1
1.000 0.040 8 10813762 intron variant G/A snv 0.61 1
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 6
rs4773144
COL4A1 ; COL4A2
0.827 0.080 13 110308365 intron variant A/G snv 0.42 1
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 3
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 7
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 5
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 21
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs2075291
APOA5 ; ZPR1
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 4
rs3135506
APOA5
0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 3
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 4
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs198389
NPPB
0.776 0.240 1 11859214 upstream gene variant A/G snv 0.39 1
rs11781551
LOC105375733
1.000 0.040 8 122395852 intergenic variant G/A snv 0.40 1
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs10846744
SCARB1
0.763 0.160 12 124827879 intron variant G/C snv 0.32 1
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 1
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 12
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 13
rs12190287
TCF21
0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 2