Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9905793
HOXB3 ; HOXB-AS3
1.000 0.040 17 48558287 intron variant A/G snv 0.86 1
rs9831002 1.000 0.040 3 18811205 intron variant T/G snv 0.59 1
rs9793739
LINC02815 ; LINC02814
1.000 0.040 1 229150111 intron variant G/A snv 9.6E-02 1
rs9366651
LOC107986582
1.000 0.040 6 26336468 upstream gene variant G/T snv 0.49 1
rs931608
ZNF98
1.000 0.040 19 22431320 intron variant A/C;T snv 2
rs9308447 1.000 0.040 1 9372331 downstream gene variant C/T snv 0.27 1
rs898797
LOC105379231 ; LOC105379230
1.000 0.040 8 9372179 intron variant C/G;T snv 1
rs8054556
TMEM219
0.925 0.080 16 29946895 intron variant G/A;C;T snv 4
rs80270335
ALK
1.000 0.040 2 29393789 intron variant C/T snv 6.5E-02 1
rs7918807 1.000 0.040 10 9978231 intergenic variant T/C snv 0.53 1
rs7852129
PCA3 ; PRUNE2
1.000 0.040 9 76731288 intron variant A/C snv 0.17 1
rs7738851
NEDD9
1.000 0.040 6 11241555 intron variant A/C;T snv 1
rs7429279
RARB
1.000 0.040 3 25077146 intron variant A/C;G snv 1
rs72748935
CA12
1.000 0.040 15 63347217 intron variant T/C snv 0.39 1
rs72694438 1.000 0.040 1 103822256 intergenic variant G/A snv 0.18 1
rs7217268
LINC00511 ; LINC02003
1.000 0.040 17 72341986 intron variant A/G;T snv 1
rs6495046
NEO1
1.000 0.040 15 73060834 intron variant C/G snv 0.71 1
rs635808
RPS6KA2
1.000 0.040 6 166763934 intron variant G/A snv 0.27 1
rs62106258 1.000 0.040 2 417167 upstream gene variant T/C snv 2.9E-02 5
rs61790808
STAG1
1.000 0.040 3 136724166 intron variant A/G snv 0.40 1
rs5922945 1.000 0.040 X 84268007 intergenic variant C/T snv 0.25 1
rs5831974
AAK1
1.000 0.040 2 69477204 intron variant -/A delins 0.60 1
rs57067187
LOC100130370
1.000 0.040 17 81387532 non coding transcript exon variant T/C snv 0.28 1
rs55769264
CDH9
1.000 0.040 5 26927939 intron variant G/A snv 0.32 1
rs4971099
TRIM46
1.000 0.040 1 155183132 intron variant A/C;G;T snv 1