Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs784257
LOC105372130
1.000 0.080 18 55729968 intron variant T/A;C snv 4
rs2236295
ADO
10 62805132 missense variant G/C;T snv 0.32 2
rs45551835
CUBN
1.000 0.080 10 16890385 missense variant G/A;T snv 1.3E-02; 4.0E-06 2
rs67339103
LRMDA
10 76133928 intron variant G/A;C;T snv 2
rs10207567
ICA1L
2 202850250 intron variant G/A;C snv 1
rs1124694
LINC02752
11 11077129 intron variant A/G;T snv 1
rs11264327 1 155122631 downstream gene variant G/A;C;T snv 1
rs13394343 2 85527219 intergenic variant C/A;T snv 1
rs1801239
CUBN
0.827 0.160 10 16877053 missense variant T/C;G snv 8.9E-02; 8.0E-06 1
rs185291443 2 226120788 intergenic variant C/A;G snv 1
rs35572189
MIR3186 ; BAHCC1
17 81451999 missense variant G/A;C snv 0.34 1
rs4109437
FRG1-DT
4 189848068 intron variant G/A;C snv 1
rs4288924 14 68835682 intergenic variant G/A;T snv 1
rs55798132
LOC105377785
8 2808621 intron variant G/A;T snv 1
rs35311980 2 228295484 intergenic variant C/T snv 4.9E-05 1
rs35924503 2 228266570 intergenic variant T/C snv 1.5E-04 1
rs539606836
CUBN
10 16963744 intron variant G/A snv 1.7E-04 1
rs34823645
C2orf83
2 227647210 intron variant T/C snv 3.9E-04 1
rs144994089
AQP7
9 33385158 missense variant C/T snv 7.0E-04 8.2E-04 1
rs183131780
LOC105373914 ; LOC107985992
2 225820170 intergenic variant C/T snv 1.0E-03 1
rs141640975
CUBN
10 16950012 missense variant G/A snv 1.7E-03 1.5E-03 1
rs189107782
FRG1-DT
4 189807855 intron variant C/T snv 1.5E-03 1
rs144360241
CUBN
10 16925418 missense variant T/C snv 5.6E-03 5.3E-03 1
rs17368443
SBF2
11 10275289 intron variant G/C snv 5.3E-02 1
rs112607182 3 170309619 downstream gene variant C/T snv 5.3E-02 2