Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11175194
SRGAP1
0.925 0.120 12 63871057 intron variant G/A snv 0.15 1
rs12039431
RSPO1
1.000 0.120 1 37616450 intron variant G/A snv 0.24 0.21 1
rs17130142
PKN2-AS1
1.000 0.120 1 87773925 intron variant G/A snv 6.5E-02 1
rs7230264 1.000 0.120 18 27347470 intron variant G/A snv 0.15 1
rs9283636 1.000 0.120 3 166315136 intergenic variant G/A snv 0.46 1
rs7405776
HNF1B
0.807 0.120 17 37733029 intron variant G/A;C snv 3
rs1413299
COL15A1
0.925 0.120 9 98998959 intron variant G/A;T snv 1
rs74917072
UBE2F ; UBE2F-SCLY
0.882 0.120 2 238022053 intron variant G/A;T snv 1
rs7643459
LOC101927394 ; LMCD1-AS1
0.925 0.120 3 7963141 intron variant G/C;T snv 1
rs7651446
TIPARP
0.882 0.120 3 156689208 intron variant G/T snv 7.9E-02 2
rs1192691 0.925 0.120 10 36880367 regulatory region variant G/T snv 0.90 1
rs1243180
MLLT10
0.790 0.160 10 21626690 intron variant T/A snv 0.23 2
rs7748275 0.882 0.120 6 3580855 downstream gene variant T/A snv 8.2E-02 1
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 1
rs11651755
HNF1B
0.763 0.160 17 37739849 intron variant T/C snv 0.52 4
rs3814113 0.827 0.200 9 16915023 upstream gene variant T/C snv 0.41 2
rs1574560 1.000 0.120 3 166329716 intergenic variant T/C snv 0.42 1
rs192876988
LOC105377300
0.851 0.120 4 79376097 intergenic variant T/C snv 1.6E-02 1
rs2660753 0.790 0.240 3 87061524 intergenic variant T/C snv 0.76 1
rs633862 0.925 0.120 9 133279871 upstream gene variant T/C snv 0.49 1
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 1
rs9787692 1.000 0.120 10 8603200 intergenic variant T/G snv 0.30 1