Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2284746
MFAP2
1 16980180 intron variant C/A;G snv 4
rs1036429
SNRPF ; CCDC38
12 95877650 intron variant T/C snv 0.79 3
rs11001819
LRMDA
10 76555466 intron variant G/A snv 0.41 3
rs11168048
LOC107986462 ; HTR4
5 148462790 intron variant T/C snv 0.38 3
rs12447804
MMP15
16 58041378 intron variant C/T snv 0.18 3
rs12477314 2 238955452 regulatory region variant C/G;T snv 3
rs12899618
THSD4
15 71352781 intron variant G/A snv 0.14 3
rs1435867
LINC01807
2 228646213 intron variant T/C snv 7.3E-02 3
rs16909898
PTCH1 ; LOC100507346
9 95468726 intron variant A/G snv 8.4E-02 0.10 3
rs17331332
INTS12
4 105886950 intron variant G/A snv 4.5E-02 3
rs1928168
CASC15
6 22017509 intron variant T/C snv 0.36 3
rs2045517
LOC105377327 ; FAM13A
4 88949813 intron variant C/T snv 0.49 3
rs2277027
ADAM19
5 157505368 intron variant A/C snv 0.42 3
rs2798641
ARMC2
6 108946847 intron variant C/T snv 0.15 3
rs2904259
FAM13A
4 88964563 intron variant T/A;C snv 3
rs3748069
ADGRG6
6 142446496 downstream gene variant A/G snv 0.39 3
rs3817928
ADGRG6
6 142429379 intron variant A/G snv 0.20 3
rs4896582
ADGRG6
6 142382740 intron variant G/A snv 0.50 3
rs7763064 6 142476152 intergenic variant G/A snv 0.38 3
rs10021465
FAM13A
4 88829210 intron variant A/G snv 0.37 2
rs10050159
GSTCD ; INTS12
4 105844758 intron variant G/A snv 0.11 2
rs10050333
INTS12 ; GSTCD
4 105844656 intron variant T/A snv 0.11 2
rs10078178
ADAM19
5 157505976 intron variant A/T snv 0.42 2
rs1032295
LOC105377462
4 144513432 intron variant T/G snv 0.32 2
rs1032297
LOC105377462
4 144513592 intron variant A/G snv 0.33 2