Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17368443
SBF2
11 10275289 intron variant G/C snv 5.3E-02 1
rs1124694
LINC02752
11 11077129 intron variant A/G;T snv 1
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs7670121
NR3C2
4 148207444 intron variant A/G snv 0.24 1
rs6535594
NR3C2
4 148211605 intron variant G/A snv 0.54 2
rs11264327 1 155122631 downstream gene variant G/A;C;T snv 1
rs1801239
CUBN
0.827 0.160 10 16877053 missense variant T/C;G snv 8.9E-02; 8.0E-06 1
rs45551835
CUBN
1.000 0.080 10 16890385 missense variant G/A;T snv 1.3E-02; 4.0E-06 2
rs144360241
CUBN
10 16925418 missense variant T/C snv 5.6E-03 5.3E-03 1
rs1276720
CUBN
10 16929427 intron variant C/T snv 0.65 1
rs141640975
CUBN
10 16950012 missense variant G/A snv 1.7E-03 1.5E-03 1
rs539606836
CUBN
10 16963744 intron variant G/A snv 1.7E-04 1
rs112607182 3 170309619 downstream gene variant C/T snv 5.3E-02 2
rs12727104 1 171454028 intergenic variant G/A snv 8.3E-02 1
rs4410790
LOC101927609 ; AHR
0.882 0.160 7 17244953 intron variant T/C snv 0.54 5
rs189107782
FRG1-DT
4 189807855 intron variant C/T snv 1.5E-03 1
rs4109437
FRG1-DT
4 189848068 intron variant G/A;C snv 1
rs12727980
LINC00862
1 200289967 intron variant C/T snv 0.54 1
rs10207567
ICA1L
2 202850250 intron variant G/A;C snv 1
rs6712846 2 207024356 intergenic variant G/A snv 0.53 1
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs183131780
LOC105373914 ; LOC107985992
2 225820170 intergenic variant C/T snv 1.0E-03 1
rs185291443 2 226120788 intergenic variant C/A;G snv 1
rs35483183
COL4A4
2 227011971 intron variant G/A snv 8.4E-02 1
rs34823645
C2orf83
2 227647210 intron variant T/C snv 3.9E-04 1