Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10862344
PPFIA2
1.000 0.040 12 81697021 intron variant A/C snv 0.98 1
rs6511404
ZNF730
1.000 0.040 19 23105059 intron variant G/A snv 0.98 1
rs7507433
ZNF730
1.000 0.040 19 23121779 intron variant G/A snv 0.98 1
rs2446597
FRMD4A
1.000 0.040 10 14007605 intron variant A/G snv 0.98 1
rs4486987
ARHGAP28
1.000 0.040 18 6762371 intron variant G/A snv 0.98 1
rs330033 1.000 0.040 8 9243439 intron variant G/A snv 0.98 1
rs9840264
FOXP1
1.000 0.040 3 71141552 intron variant G/A snv 0.98 1
rs243391
UBXN6
1.000 0.040 19 4449811 non coding transcript exon variant G/A snv 0.98 1
rs2053762
LOC105373845
1.000 0.040 2 204472387 intron variant A/G snv 0.98 1
rs1885645 1.000 0.040 1 177768233 intron variant A/G snv 0.98 1
rs12472508 1.000 0.040 2 204456249 intergenic variant G/A snv 0.98 1
rs3848860
MYO18B
1.000 0.040 22 25790224 intron variant C/T snv 0.98 1
rs2842861
SLC25A44
1.000 0.040 1 156202708 intron variant T/C snv 0.98 1
rs3102718
SCAPER
1.000 0.040 15 76752585 intron variant C/T snv 0.98 1
rs198260 1.000 0.040 14 56714297 intron variant G/A snv 0.98 1
rs622180 1.000 0.040 19 56080944 downstream gene variant T/C snv 0.98 1
rs4273150
C19orf47
1.000 0.040 19 40308106 regulatory region variant C/T snv 0.97 1
rs2670473
DIAPH3
1.000 0.040 13 60078156 intron variant A/G snv 0.97 1
rs1550910 1.000 0.040 2 204470907 intron variant C/T snv 0.97 1
rs792605 1.000 0.040 8 13941525 intergenic variant G/T snv 0.97 1
rs9542861 1.000 0.040 13 72147047 intergenic variant T/A snv 0.97 1
rs1910462
IQCM
1.000 0.040 4 149509171 intron variant G/A snv 0.97 1
rs820274
GBE1
1.000 0.040 3 81496552 intron variant A/G snv 0.97 1
rs2959611
ZDHHC2
1.000 0.040 8 17218181 intron variant G/A snv 0.97 1
rs2718796
TF
1.000 0.040 3 133760356 non coding transcript exon variant G/C snv 0.97 1