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
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 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
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 18
rs174533
MYRF ; TMEM258
0.763 0.160 11 61781553 intron variant G/A snv 0.37 0.29 17
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 17
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 16
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 14
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 13
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 12
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 12
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 11
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 10
rs516246
FUT2 ; LOC105447645
0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 10
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 9
rs174577
FADS2
1.000 0.080 11 61837342 intron variant C/A snv 0.38 9
rs2740488
ABCA1
0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
rs2954031 8 125479491 intron variant G/T snv 0.42 8
rs4665972
SNX17
2 27375230 intron variant T/C snv 0.69 8
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7