Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs7950273
PDGFD
0.925 0.120 11 104160870 intron variant C/G snv 0.32 1
rs9282541
ABCA1
0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 2
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 3
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 19
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 16
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 7
rs7690819 1.000 0.040 4 111199502 intergenic variant A/G;T snv 3
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs11066001
BRAP
0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 3
rs4374383
MERTK
0.776 0.200 2 112013193 intron variant A/G snv 0.58 3
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 13
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 1
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 1
rs11196172
TCF7L2
0.708 0.200 10 112967084 intron variant G/A snv 0.13 9
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 18
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs7080536
HABP2 ; NRAP
0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 3
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs17137004
FOXP2
1.000 0.040 7 114389196 intron variant A/G snv 0.38 2
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
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
rs5128
APOC3
0.925 0.080 11 116832924 3 prime UTR variant G/C snv 0.84 0.87 1
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv 16