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
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 16
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
rs6058093
PIGU
0.776 0.080 20 34625392 intron variant A/C snv 0.55 12
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 9
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 8
rs10224210
PRKAG2
1.000 0.040 7 151716108 intron variant T/C snv 0.21 8
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 7
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs35789010
CARMIL1
0.851 0.200 6 25513951 intron variant G/A snv 4.1E-02 7
rs3765209
LOC101927745
0.851 0.040 21 15417030 intron variant C/T snv 0.31 7
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 7
rs77924615
PDILT
1.000 0.080 16 20381010 intron variant G/A snv 0.16 7
rs13146355
SHROOM3
1.000 0.040 4 76490987 intron variant G/A snv 0.33 6
rs13333226
UMOD
0.827 0.200 16 20354332 intron variant A/G snv 0.23 6
rs7740107
L3MBTL3
1.000 0.080 6 130053316 intron variant T/A;G snv 6
rs9472135
LOC107986598
0.925 0.120 6 43842065 intron variant T/A;C;G snv 6
rs11072567
NRG4
15 76006403 intron variant A/G snv 0.43 5
rs11755724
RREB1
0.807 0.320 6 7118757 intron variant A/G;T snv 5
rs2823139 1.000 0.080 21 15204463 intron variant G/A snv 0.34 5
rs4410790
LOC101927609 ; AHR
0.882 0.160 7 17244953 intron variant T/C snv 0.54 5
rs8096658
NFATC1 ; LOC107985163
0.925 0.120 18 79396537 intron variant C/G snv 0.39 5