Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11291804 17 30305102 intergenic variant TTTT/-;T;TT;TTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTTTTTT delins 1
rs34208856
HBS1L
6 135099930 intron variant TT/-;T;TTT;TTTTTTTTT delins 6
rs77987196
GPAM
10 112173249 intron variant TT/-;T;TTT delins 0.71 2
rs661171
ZC3H12C ; RDX
11 110145794 intron variant T/G snv 0.69 5
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 4
rs5942937 X 110473179 intron variant T/G snv 0.47 4
rs3850634
DOCK7
1 62584927 intron variant T/G snv 0.33 0.34 3
rs4082919
PGS1
17 78381401 intron variant T/G snv 0.55 3
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 3
rs3786247
LIPG
18 49592553 3 prime UTR variant T/G snv 0.13 2
rs3843482
HMGCR
5 75343434 intron variant T/G snv 0.35 2
rs9357121
HLA-B ; HLA-C
6 31272702 intron variant T/G snv 3.5E-02 2
rs9923854
CETP
16 56983090 intron variant T/G snv 0.10 2
rs9939224
CETP
1.000 0.040 16 56968820 intron variant T/G snv 0.75 2
rs314311
EPHB4
7 100824859 non coding transcript exon variant T/G snv 0.17 1
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 1
rs57594838 10 112265424 intergenic variant T/G snv 0.24 1
rs6435161
FAM117B
2 202655060 intron variant T/G snv 0.23 1
rs672889 2 21096144 intron variant T/G snv 0.80 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs4722551
LOC105375199
7 25952206 upstream gene variant T/C;G snv 4
rs12916
HMGCR ; CERT1
0.807 0.240 5 75360714 3 prime UTR variant T/C;G snv 0.37 3
rs4939883
LOC105372112
1.000 0.040 18 49640844 TF binding site variant T/C;G snv 3
rs8078686
KPNB1
17 47658340 intron variant T/C;G snv 0.49 3
rs2807834
MTARC1
1 220797251 intron variant T/C;G snv 2