Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2866611 0.851 0.120 20 41322165 upstream gene variant A/T snv 0.58 16
rs760762
PLCG1
0.851 0.120 20 41147406 intron variant C/A;T snv 0.59 16
rs127430
APCDD1L-DT
20 58589799 intron variant A/G;T snv 5
rs6059932
PIGU
20 34587662 intron variant C/T snv 0.44 4
rs6065906 20 45925376 downstream gene variant T/A;C;G snv 4
rs7679
PCIF1
0.925 0.160 20 45947863 3 prime UTR variant T/C snv 0.13 4
rs4465830
ZNF335
20 45956781 intron variant A/G snv 0.13 3
rs4810479 1.000 0.040 20 45916409 upstream gene variant C/T snv 0.68 3
rs6065904
PLTP
1.000 0.080 20 45906012 intron variant G/A snv 0.23 3
rs6073958 20 45923216 downstream gene variant T/C snv 0.22 3
rs184392658
PIGT ; LOC105372631
20 45438925 intron variant T/C snv 3.0E-03 2
rs4911477
PROCR ; MMP24-AS1-EDEM2
20 35193182 intron variant T/C snv 0.38 2
rs6073972
ZNF335
20 45961659 non coding transcript exon variant C/G snv 0.13 2
rs6130975
PCIF1 ; ZNF335
20 45948343 downstream gene variant G/A;C snv 2
rs76083992 20 45916159 upstream gene variant C/T snv 3.5E-02 2
rs141588480
SNTA1
20 33426108 intron variant T/- del 1.7E-02 1
rs143876112
RBM39
20 35712465 intron variant C/G;T snv 1
rs2281279
SULF2
20 47661506 non coding transcript exon variant T/C snv 0.25 1
rs3746428
MMP24-AS1-EDEM2 ; EDEM2
20 35131380 intron variant G/A snv 0.14 1
rs435306
PLTP
20 45909845 intron variant G/T snv 0.71 1
rs562306828 20 45928576 non coding transcript exon variant -/G;GAG;GAGAG ins 1
rs6059988
NCOA6 ; PIGU
20 34690297 intron variant T/C snv 0.41 1
rs6120815 20 31597063 regulatory region variant T/C snv 0.27 1
rs6124760
ZNF335
20 45952814 intron variant C/G snv 4.7E-02 1
rs856404
LINC01524 ; LOC105372666
20 52647247 non coding transcript exon variant G/A snv 0.63 1