Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10757269
CDKN2B-AS1
1.000 0.040 9 22072265 intron variant A/C;G snv 1
rs16939881
ALDH1A2 ; AQP9
15 58179780 intron variant G/C;T snv 1
rs3809346
COL4A1 ; COL4A2
1.000 0.080 13 110308596 intron variant G/A;C snv 1
rs4977575
CDKN2B-AS1
1.000 0.040 9 22124745 intron variant C/G;T snv 1
rs7092929
LOC105376360 ; LINC02669
10 3496602 splice region variant A/C;T snv 1
rs9632884
CDKN2B-AS1
0.851 0.160 9 22072302 intron variant G/A;C snv 1
rs4272321
PTPRN2
1.000 0.080 7 158159143 intron variant A/G snv 4.6E-04 2
rs1998013 1 55492357 intron variant C/T snv 4.4E-03 1
rs115689251
LOC107985068
1.000 0.080 17 36032377 intergenic variant A/C snv 1.0E-02 2
rs59811240
MTSS1
1.000 0.080 8 124709787 intron variant C/A snv 1.3E-02 2
rs76294234 1.000 0.080 4 83241025 intron variant A/G snv 1.5E-02 2
rs114031744 1.000 0.080 10 123610085 intergenic variant A/G snv 1.7E-02 2
rs113533135
LRP1B
1.000 0.080 2 140268867 intron variant T/C snv 2.0E-02 2
rs1532002
LRP1B
1.000 0.080 2 140292500 intron variant G/A snv 2.3E-02 2
rs74155456 1.000 0.080 10 61070020 intergenic variant T/C snv 2.3E-02 2
rs73169578 1.000 0.080 13 21120420 intergenic variant G/A snv 3.1E-02 2
rs74910095 1.000 0.080 5 63545132 intergenic variant T/A snv 3.7E-02 2
rs77757620
STARD9
1.000 0.080 15 42661399 intron variant C/T snv 3.8E-02 2
rs74570061
ARL9
1.000 0.080 4 56517605 intron variant T/C snv 3.9E-02 2
rs16850360 4 74006728 intron variant A/G snv 4.2E-02 1
rs2168889 4 74357994 intergenic variant A/G snv 4.7E-02 1
rs9973676
GPR55
1.000 0.080 2 230954091 intron variant G/A snv 5.8E-02 2
rs741013
PRICKLE2
3 64306961 intron variant A/T snv 6.0E-02 1
rs113805659
MAGI2
1.000 0.080 7 78663475 intron variant G/C snv 6.1E-02 2
rs10502575 18 31756628 downstream gene variant A/G snv 6.9E-02 1