Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2540913
MIR4432HG
2 60383677 non coding transcript exon variant T/C snv 0.30 3
rs2540916
MIR4432HG
2 60381795 intron variant T/A;C snv 3
rs2540917
MIR4432HG
2 60381624 intron variant T/C snv 0.29 3
rs2668729
MIR4432HG
2 60381248 intron variant G/A snv 0.39 3
rs925483
MIR4432HG
2 60384150 intron variant G/A snv 0.29 3
rs925484
MIR4432HG
2 60384302 intron variant C/A;G snv 3
rs9967849
MIR4432HG
2 60382339 intron variant C/T snv 0.33 3
rs11036238 1.000 0.040 11 5204405 upstream gene variant G/C snv 0.21 2
rs11125842 2 60413672 intron variant A/G snv 0.49 2
rs11884411 2 60442359 upstream gene variant T/C snv 0.51 2
rs11894442 2 60429883 intron variant T/C snv 0.51 2
rs12104736 2 60423581 intron variant C/G snv 0.48 2
rs12474693 2 60441297 upstream gene variant C/G;T snv 2
rs243065 2 60394929 intron variant G/C snv 0.45 2
rs10189857
BCL11A
1.000 0.080 2 60486100 intron variant A/G snv 0.42 2
rs13019832
BCL11A
2 60483436 intron variant G/A snv 0.39 2
rs7606173
BCL11A
1.000 0.080 2 60498316 intron variant G/C;T snv 0.39 2
rs4910742
HBG2 ; HBE1
11 5285279 intron variant G/A;T snv 2
rs13011022
LOC102724142
2 60399687 intron variant G/A snv 0.35 2
rs888082
LOC102724142
2 60402474 intron variant G/A snv 0.48 2
rs243078
MIR4432 ; MIR4432HG
2 60388168 intron variant A/G snv 0.42 2
rs243081
MIR4432HG
2 60386641 intron variant G/A snv 0.41 2
rs243079
MIR4432HG ; MIR4432
2 60387893 intron variant A/C snv 0.42 2
rs12789492
MMP26
1.000 0.040 11 4772889 intron variant C/T snv 9.6E-02 2
rs17228092
MMP26
1.000 0.040 11 4789134 intron variant T/C snv 9.6E-02 2