Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10757272
CDKN2B-AS1
0.851 0.160 9 22088261 intron variant C/T snv 0.41 2
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 2
rs1333037
CDKN2B-AS1
0.925 0.040 9 22040766 intron variant C/T snv 0.71 2
rs1333040
CDKN2B-AS1
0.732 0.280 9 22083405 intron variant C/G;T snv 2
rs1333042
CDKN2B-AS1
0.827 0.120 9 22103814 intron variant A/G snv 0.63 2
rs2891168
CDKN2B-AS1
0.851 0.160 9 22098620 intron variant A/G snv 0.40 2
rs564398
CDKN2B-AS1
0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 2
rs7859727
CDKN2B-AS1
1.000 0.080 9 22102166 intron variant C/T snv 0.57 2
rs7865618
CDKN2B-AS1
0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 2
rs448792
FRY
1.000 0.080 13 32103287 intron variant T/A;C snv 2
rs543554
FRY
1.000 0.080 13 32127501 intron variant A/G;T snv 2
rs6606859
GABRG3
1.000 0.080 15 27032254 intron variant C/A;T snv 2
rs9973676
GPR55
1.000 0.080 2 230954091 intron variant G/A snv 5.8E-02 2
rs1912826
KLKB1
4 186228386 intron variant G/A;C snv 2
rs8134546
LINC01426
1.000 0.080 21 34782568 intron variant T/C snv 8.7E-02 2
rs4788815
LOC105371334
16 71600908 intergenic variant A/T snv 0.69 2
rs6506900
LOC105372049
1.000 0.080 18 31226433 intergenic variant A/C;G snv 2
rs9384331
LOC105378054
1.000 0.080 6 150279905 intergenic variant T/C snv 0.12 2
rs115689251
LOC107985068
1.000 0.080 17 36032377 intergenic variant A/C snv 1.0E-02 2
rs6754498
LOC107985783
1.000 0.080 2 185953121 non coding transcript exon variant A/C;G;T snv 2
rs91
LOC107986777
1.000 0.080 7 24409992 intron variant T/C snv 0.41 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
rs113805659
MAGI2
1.000 0.080 7 78663475 intron variant G/C snv 6.1E-02 2
rs59811240
MTSS1
1.000 0.080 8 124709787 intron variant C/A snv 1.3E-02 2