Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1291621
SCAF11
1.000 0.040 12 45947038 intron variant A/G snv 0.98 1
rs2266788
APOA5 ; ZPR1
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 6
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 1
rs3130683
C2 ; CYP21A2
1.000 0.040 6 31920590 intron variant C/T snv 0.91 1
rs12493885
ARHGEF26-AS1 ; ARHGEF26
1.000 0.040 3 154122077 missense variant G/C snv 0.91 0.91 1
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 4
rs505151
PCSK9
0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 2
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 10
rs1629862
EDN1
1.000 0.040 6 12295643 intron variant A/G snv 0.89 1
rs430918 1.000 0.040 6 57249018 intergenic variant C/T snv 0.87 1
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 1
rs7797644
KDELR2 ; DAGLB
1.000 0.040 7 6446436 intron variant T/C snv 0.84 1
rs2288904
SLC44A2
0.807 0.240 19 10631494 missense variant A/G snv 0.80 0.83 2
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 1
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs2257129
LOC105378522
1.000 0.040 10 121139183 regulatory region variant T/C snv 0.82 3
rs585967 1.000 0.040 2 21047682 upstream gene variant A/C snv 0.81 1
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 11
rs2227564
PLAU ; C10orf55
0.763 0.320 10 73913343 missense variant T/C snv 0.75 0.81 3
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 10
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 7
rs1250259
FN1 ; LOC105373868
1.000 0.040 2 215435759 missense variant T/A snv 0.76 0.79 5
rs4845570
TDRKH
1.000 0.040 1 151786628 intron variant C/T snv 0.79 1
rs56079296 1.000 0.040 5 121941102 intergenic variant A/G snv 0.78 1
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 8