Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4846044
C1orf167-AS1 ; C1orf167
1 11779941 missense variant T/C;G snv 0.95 2
rs1352714
DCHS2
0.925 0.280 4 154322452 missense variant T/C snv 0.95 0.90 2
rs505151
PCSK9
0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 2
rs1663564
WASHC4
12 105152394 missense variant G/A snv 0.95 0.95 1
rs3096380
CMTR2
1.000 0.080 16 71285743 missense variant G/A;C snv 0.94 1
rs7698623
MEPE
4 87834676 intron variant T/A;C snv 6.1E-05; 0.94 1
rs619865
MMP24-AS1-EDEM2 ; MMP24OS ; EIF6
1.000 0.040 20 35279894 intron variant A/G snv 0.94 0.94 1
rs4725617
EPHA1
7 143400007 missense variant A/G;T snv 0.93 1
rs3851294
DSTYK
1 205161285 missense variant A/G;T snv 0.93 2
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs2276749
VGLL4
3 11601991 missense variant T/A;C snv 8.5E-06; 0.93 1
rs942637
ITPR3
1.000 0.080 6 33685334 intron variant T/A;C snv 0.92 2
rs4668356
GORASP2
2 170965956 synonymous variant C/G;T snv 2.2E-03; 0.92 1
rs249038
ZFYVE16
1.000 0.040 5 80449650 missense variant A/G snv 0.91 0.87 1
rs6042507
SIRPB2
20 1478415 missense variant T/A;C;G snv 9.6E-05; 4.0E-06; 0.91 1
rs808919
ANKRD52
12 56254127 synonymous variant G/C;T snv 0.91; 2.4E-05 1
rs10063424
FOXI1
1.000 0.040 5 170108518 synonymous variant T/C snv 0.91 0.90 1
rs1484873
SLC14A2
18 45627020 missense variant A/C;G snv 0.91 1
rs12493885
ARHGEF26-AS1 ; ARHGEF26
1.000 0.040 3 154122077 missense variant G/C snv 0.91 0.91 1
rs611779
ADGRF5
6 46859173 synonymous variant G/A;T snv 0.91 1
rs1499280
PELO ; ITGA1
5 52801055 missense variant C/A snv 0.91 0.91 1
rs1552286
NUDT18
8 22107291 3 prime UTR variant C/T snv 0.90 0.88 1
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 25
rs35381162
HMGA1
6 34243565 intron variant T/- delins 0.90 0.86 1
rs629849
IGF2R
0.827 0.160 6 160073377 missense variant A/C;G;T snv 0.90 0.91 1