Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs201286260 11 5205088 splice donor variant -/A ins 1
rs243079
MIR4432HG ; MIR4432
2 60387893 intron variant A/C snv 0.42 2
rs12477097
BCL11A
2 60471262 intron variant A/C snv 0.30 1
rs2647602
OR52H2P
11 5552471 non coding transcript exon variant A/C snv 0.37 1
rs4348933
HBG2
11 5263748 intron variant A/C;G snv 1
rs4671393
BCL11A
0.790 0.400 2 60493816 intron variant A/C;G snv 1
rs6545816
BCL11A
1.000 0.080 2 60487726 intron variant A/C;G snv 0.50 1
rs4758622
NAP1L4
11 2988691 intron variant A/C;G;T snv 1
rs431117 11 5553050 intron variant A/C;T snv 1
rs934460
UBQLNL
11 5513952 intron variant A/C;T snv 1
rs4895441
LOC105378010
0.925 0.080 6 135105435 upstream gene variant A/G snv 0.21 7
rs1320963 6 135122074 intergenic variant A/G snv 0.35 5
rs243066 2 60394631 intron variant A/G snv 0.29 3
rs10189857
BCL11A
1.000 0.080 2 60486100 intron variant A/G snv 0.42 2
rs11125842 2 60413672 intron variant A/G snv 0.49 2
rs12788102
MMP26 ; OR51F1
1.000 0.040 11 4769345 synonymous variant A/G snv 9.5E-02 9.6E-02 2
rs17228176
MMP26
1.000 0.040 11 4790570 intron variant A/G snv 9.6E-02 2
rs243078
MIR4432 ; MIR4432HG
2 60388168 intron variant A/G snv 0.42 2
rs1044392
UBQLNL
11 5514441 3 prime UTR variant A/G snv 0.35 1
rs11037191
OR51M1 ; HBE1 ; OR51B5 ; HBG2
11 5390842 3 prime UTR variant A/G snv 4.6E-02 1
rs11039508
TRIM5 ; LOC112268071 ; OR52E5
11 5899467 intron variant A/G snv 6.5E-02 1
rs11125841
LOC102724142
2 60400430 intron variant A/G snv 0.48 1
rs12468946 2 60443342 upstream gene variant A/G snv 0.51 1
rs1318772
MCC
1.000 0.080 5 113387870 intron variant A/G snv 0.18 1
rs17227484
MMP26
11 4772652 intron variant A/G snv 9.6E-02 1