Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs217181
TXNL4B
16 72080103 intron variant C/T snv 0.20 4
rs2157719
CDKN2B-AS1
0.708 0.360 9 22033367 non coding transcript exon variant C/T snv 0.71 3
rs4810479 1.000 0.040 20 45916409 upstream gene variant C/T snv 0.68 3
rs10757272
CDKN2B-AS1
0.851 0.160 9 22088261 intron variant C/T snv 0.41 2
rs11509197 1.000 0.080 7 118641356 intergenic variant C/T snv 0.38 2
rs1333037
CDKN2B-AS1
0.925 0.040 9 22040766 intron variant C/T snv 0.71 2
rs72928364
ABI3BP
1.000 0.080 3 100894935 intron variant C/T snv 0.39 2
rs77757620
STARD9
1.000 0.080 15 42661399 intron variant C/T snv 3.8E-02 2
rs7859727
CDKN2B-AS1
1.000 0.080 9 22102166 intron variant C/T snv 0.57 2
rs10889332
DOCK7
1.000 0.120 1 62485187 3 prime UTR variant C/T snv 0.39 1
rs1537370
CDKN2B-AS1
1.000 9 22084311 intron variant C/T snv 0.55 1
rs1998013 1 55492357 intron variant C/T snv 4.4E-03 1
rs6475606
CDKN2B-AS1
0.882 0.080 9 22081851 intron variant C/T snv 0.62 1
rs749924
LINC01880
2 242084344 upstream gene variant C/T snv 0.25 1
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 5
rs10211524
LOC107984063 ; LINC02245
2 64980940 intron variant G/A snv 0.51 3
rs1532002
LRP1B
1.000 0.080 2 140292500 intron variant G/A snv 2.3E-02 2
rs59490629
PDSS2
1.000 0.080 6 107256268 intron variant G/A snv 8.5E-02 2
rs6506897 1.000 0.080 18 31215320 intergenic variant G/A snv 0.62 2
rs6898559
ALDH7A1
1.000 0.080 5 126557237 intron variant G/A snv 0.66 2
rs73169578 1.000 0.080 13 21120420 intergenic variant G/A snv 3.1E-02 2
rs9973676
GPR55
1.000 0.080 2 230954091 intron variant G/A snv 5.8E-02 2
rs10811645
CDKN2B-AS1
1.000 0.040 9 22049657 intron variant G/A snv 0.59 1
rs12507628 4 72779634 regulatory region variant G/A snv 0.13 1
rs1851024 4 71842104 intergenic variant G/A snv 0.93 1