Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34445740
SMAD3
0.925 0.080 15 67183426 intron variant -/A delins 0.29 2
rs35251008
SMAD3
15 67176187 intron variant A/C;G snv 1
rs72743477
SMAD3
0.724 0.240 15 67171953 intron variant A/G snv 0.17 14
rs35874463
SMAD3
0.827 0.120 15 67165360 missense variant A/G snv 4.0E-02 3.4E-02 7
rs17294280
SMAD3
0.882 0.120 15 67175947 intron variant A/G snv 0.19 4
rs2033784
SMAD3
1.000 0.080 15 67157322 intron variant A/G snv 0.35 3
rs17228058
SMAD3
1.000 0.040 15 67157967 intron variant A/G snv 0.17 2
rs12901071
SMAD3
0.882 0.160 15 67078051 intron variant A/G snv 0.25 1
rs4776342
SMAD3
15 67126053 intron variant A/G snv 0.30 1
rs12901372
SMAD3
1.000 0.040 15 67078168 intron variant C/A;G snv 1
rs72743461
SMAD3
0.827 0.160 15 67149412 intron variant C/A;T snv 6
rs10438355
SMAD3
15 67195211 downstream gene variant C/G snv 0.20 1
rs10152595
SMAD3
1.000 0.080 15 67183150 intron variant C/G;T snv 2
rs8025774
SMAD3
15 67190938 3 prime UTR variant C/G;T snv 1
rs11639295
SMAD3
1.000 0.040 15 67168419 intron variant C/G;T snv 1
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 8
rs56062135
SMAD3
0.790 0.200 15 67163292 intron variant C/T snv 0.18 6
rs28617673
SMAD3
1.000 0.080 15 67078906 intron variant C/T snv 0.16 1
rs12912045
SMAD3
15 67174959 intron variant C/T snv 0.25 1
rs56375023
SMAD3
0.925 0.120 15 67156025 intron variant G/A snv 0.17 3
rs117683492
SMAD3
1.000 0.080 15 67121286 intron variant G/A snv 1.2E-02 1
rs744910
SMAD3
1.000 0.080 15 67154447 intron variant G/A;T snv 1
rs2289261
SMAD3
1.000 0.080 15 67165147 intron variant G/C;T snv 0.61 1
rs12912010
SMAD3
15 67174805 intron variant G/T snv 0.24 1
rs4776879
SMAD3
15 67071982 intron variant T/A;C snv 1