Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5831974
AAK1
1.000 0.040 2 69477204 intron variant -/A delins 0.60 1
rs3114018
ABCG2
0.882 0.160 4 88143429 intron variant A/C snv 0.48 2
rs10242311
ATXN7L1
1.000 0.040 7 105633273 intron variant A/C snv 6.2E-02 1
rs7852129
PCA3 ; PRUNE2
1.000 0.040 9 76731288 intron variant A/C snv 0.17 1
rs7429279
RARB
1.000 0.040 3 25077146 intron variant A/C;G snv 1
rs4971099
TRIM46
1.000 0.040 1 155183132 intron variant A/C;G;T snv 1
rs931608
ZNF98
1.000 0.040 19 22431320 intron variant A/C;T snv 2
rs2652452
KCNJ3
1.000 0.040 2 154813691 intron variant A/C;T snv 1
rs3865314
NPEPPS
1.000 0.040 17 47592158 intron variant A/C;T snv 1
rs7738851
NEDD9
1.000 0.040 6 11241555 intron variant A/C;T snv 1
rs11676272
ADCY3
1.000 0.040 2 24918669 missense variant A/G snv 0.47 0.57 3
rs10048146 1.000 0.040 16 86677054 regulatory region variant A/G snv 0.17 2
rs10180496 1.000 0.040 2 12828774 intron variant A/G snv 0.15 1
rs10811723 1.000 0.040 9 22542286 intergenic variant A/G snv 0.55 1
rs11166135 1.000 0.040 1 98883280 intergenic variant A/G snv 0.10 1
rs61790808
STAG1
1.000 0.040 3 136724166 intron variant A/G snv 0.40 1
rs9905793
HOXB3 ; HOXB-AS3
1.000 0.040 17 48558287 intron variant A/G snv 0.86 1
rs11672900
MAMSTR
1.000 0.040 19 48717066 intron variant A/G;T snv 1
rs7217268
LINC00511 ; LINC02003
1.000 0.040 17 72341986 intron variant A/G;T snv 1
rs1352724 1.000 0.040 5 107747786 intergenic variant C/A snv 0.15 1
rs263771 1.000 0.040 2 185056965 intergenic variant C/A;T snv 1
rs6495046
NEO1
1.000 0.040 15 73060834 intron variant C/G snv 0.71 1
rs1594318
ALLC
1.000 0.040 2 3686354 intron variant C/G;T snv 1
rs3737665
CA6
0.925 0.080 1 8970905 missense variant C/G;T snv 4.0E-06; 0.26 1
rs898797
LOC105379231 ; LOC105379230
1.000 0.040 8 9372179 intron variant C/G;T snv 1