Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 22
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 20
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 18
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 16
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs174537
TMEM258 ; MYRF
0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 14
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 14
rs7137828
ATXN2
0.763 0.200 12 111494996 intron variant C/A;T snv 14
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 12
rs1537372
CDKN2B-AS1
0.752 0.120 9 22103184 intron variant G/A;T snv 11
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 11
rs61776719 0.776 0.120 1 37995647 downstream gene variant C/A snv 0.46 11
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 10
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 10
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs715
CPS1
1.000 0.040 2 210678331 3 prime UTR variant T/C snv 0.28 10
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 9