Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10259477 0.925 0.040 7 11855801 intergenic variant A/C;T snv 2
rs1027341
ZNF438
0.925 0.040 10 30885574 intron variant T/A snv 0.79 2
rs1027986
LYN
0.925 0.040 8 55969912 intron variant A/G snv 0.44 2
rs10280201 0.925 0.040 7 38637079 intergenic variant G/A;T snv 2
rs1028911
LOC100506207 ; HULC
0.925 0.040 6 8706288 intron variant T/C;G snv 2
rs1030062 0.925 0.040 X 147707185 intergenic variant T/C snv 4.0E-02 2
rs1039751
CWC15
0.925 0.040 11 94962268 downstream gene variant C/A snv 0.91 2
rs10405809
CRX
0.925 0.040 19 47823958 intron variant G/A snv 9.5E-02 2
rs10409138
PPP1R37 ; MARK4
0.925 0.040 19 45121045 intron variant A/G snv 0.15 2
rs10432510
LOC107985833
0.925 0.040 2 191522137 regulatory region variant C/T snv 0.95 2
rs10436911
LOC105371657
0.925 0.040 1 189546287 intergenic variant A/G snv 8.3E-02 2
rs10466716
DLG2 ; DLG2-AS2
0.925 0.040 11 83654900 intron variant A/G snv 9.3E-02 2
rs1046774
ZMAT1
0.925 0.040 X 101882824 3 prime UTR variant G/A;T snv 2
rs10489629
IL23R ; C1orf141
0.827 0.240 1 67222666 intron variant T/C snv 0.48 2
rs10493390
PDE4B
0.925 0.040 1 65846910 intron variant A/C snv 1.7E-02 2
rs10499658 0.925 0.040 7 47183968 intergenic variant G/A snv 0.14 2
rs10499763 0.925 0.040 7 56650806 upstream gene variant G/A snv 3.3E-02 2
rs10508115 0.925 0.040 13 103536265 intergenic variant A/G snv 3.8E-02 2
rs10510181
CHL1-AS2
0.882 0.200 3 149364 intron variant G/A snv 0.31 1
rs10514207
LOC339298
0.925 0.040 18 76143976 intron variant A/G snv 0.15 2
rs1051432
WDR59
0.925 0.040 16 74873752 3 prime UTR variant G/C snv 8.8E-02 2
rs1059214
MSMO1
0.925 0.040 4 165342308 3 prime UTR variant C/G snv 0.10 2
rs10739217
LOC107987108
0.925 0.040 9 105973112 regulatory region variant T/A;C snv 3
rs10741881
NELL1
0.925 0.040 11 21498856 intron variant C/T snv 0.98 2
rs10748401
NELL2
0.925 0.040 12 44758763 intron variant A/C snv 0.71 2