Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17032384
LINC02456 ; HELLPAR
0.925 0.040 12 102283136 non coding transcript exon variant T/G snv 3.9E-02 2
rs1372812
SBF2
0.925 0.040 11 10233236 intron variant T/C snv 2.2E-02 2
rs13330098
LOC105371078
0.925 0.040 16 10236420 intergenic variant T/C snv 5.9E-02 2
rs28634469 0.925 0.040 2 102399706 downstream gene variant C/T snv 3.6E-02 2
rs6571017 0.925 0.040 6 102437755 intergenic variant G/A;T snv 2
rs7953558
KLRD1
0.925 0.040 12 10246509 intron variant C/G;T snv 2
rs6752950
TMEM182
0.925 0.040 2 102816833 3 prime UTR variant C/A;G snv 4.5E-02 2
rs10508115 0.925 0.040 13 103536265 intergenic variant A/G snv 3.8E-02 2
rs7138824
STAB2
0.925 0.040 12 103714729 intron variant C/T snv 0.13 2
rs6965019
RELN
0.925 0.040 7 103758220 intron variant A/G snv 2.2E-02 2
rs17034117 0.925 0.040 4 103845100 intergenic variant G/C snv 2.4E-02 2
rs1885073 0.925 0.040 14 103890845 intergenic variant A/G;T snv 2
rs4698925 0.925 0.040 4 104770586 intron variant C/T snv 0.25 2
rs4895110
LOC107986108
0.925 0.040 3 104884995 intergenic variant A/C;G;T snv 2
rs10884064
SORCS3
0.925 0.040 10 104913316 intron variant T/C snv 0.50 2
rs7633661
ATP2B2
0.925 0.040 3 10508163 intron variant C/T snv 9.6E-02 2
rs2784598
PTPRD
0.925 0.040 9 10512307 intron variant T/A;C snv 2
rs11192399 0.925 0.040 10 105324556 intergenic variant A/G snv 8.4E-02 2
rs17119235 0.925 0.040 10 105635233 intergenic variant G/C snv 3.6E-02 2
rs17036090
ARHGEF38
0.925 0.040 4 105672417 intron variant T/C snv 5.0E-02 2
rs1086512 0.925 0.040 1 105694496 upstream gene variant G/T snv 2.0E-02 2
rs17036152
GSTCD ; INTS12
0.925 0.040 4 105741819 intron variant T/C snv 7.6E-03 2
rs12296982 0.925 0.040 12 105820730 regulatory region variant C/T snv 0.10 2
rs10739217
LOC107987108
0.925 0.040 9 105973112 regulatory region variant T/A;C snv 3
rs2866784
NPNT
0.925 0.040 4 105992198 intron variant T/C snv 0.14 2