Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10795656 1.000 0.080 10 8553876 intergenic variant G/A;T snv 4
rs7512552
MRPS21 ; LOC105371434
1.000 0.120 1 150293284 upstream gene variant T/C snv 0.63 4
rs2033784
SMAD3
1.000 0.080 15 67157322 intron variant A/G snv 0.35 3
rs2164068
PLCL1
1.000 0.120 2 198079128 intron variant T/A snv 0.52 3
rs2381416 1.000 0.080 9 6193455 upstream gene variant C/A snv 0.65 3
rs301805
RERE
1.000 0.080 1 8420956 intron variant T/G snv 0.65 3
rs36045143
LOC105371081 ; CLEC16A
1.000 0.080 16 11131109 intron variant A/G snv 0.18 3
rs6489785 1.000 0.040 12 120925921 TF binding site variant T/C snv 0.68 3
rs71368508
LOC105371498
1.000 0.040 17 4618178 downstream gene variant C/A snv 1.7E-02 3
rs10008032
LOC105374413
1.000 0.080 4 38743861 intergenic variant T/C snv 0.66 2
rs10074523
KIF3A
1.000 0.080 5 132724891 intron variant C/A snv 0.62 2
rs1017494 1.000 0.080 2 234770601 regulatory region variant C/A;G;T snv 2
rs10174949
LINC00299
1.000 0.080 2 8302118 non coding transcript exon variant G/A snv 0.23 2
rs10455025
TSLP
1.000 0.080 5 111069301 upstream gene variant A/C snv 0.24 2
rs10910095
LOC100996583
1.000 0.040 1 2579316 upstream gene variant G/A;C snv 2
rs10947428
ITPR3
1.000 0.040 6 33679281 intron variant T/C snv 0.26 2
rs11169225
AQP2 ; LOC101927318
1.000 0.120 12 49951888 intron variant T/A snv 0.13 2
rs11255753 1.000 0.040 10 8563590 intergenic variant G/C;T snv 0.23 2
rs11644510
CLEC16A
1.000 0.120 16 11183501 downstream gene variant C/T snv 0.39 2
rs11645657
LOC105371081 ; CLEC16A
1.000 0.080 16 11129597 intron variant C/A;G snv 0.48 2
rs12339348
LOC107987046 ; IL33
1.000 0.080 9 6233082 intron variant A/G;T snv 2
rs1241357 1.000 0.080 8 56793197 intergenic variant G/A snv 2
rs12743520
EVI5
1.000 0.080 1 92571555 intron variant C/A snv 0.20 2
rs13001325
IL18R1 ; IL1RL1
1.000 0.040 2 102322576 intron variant C/T snv 0.30 2
rs13099273
LPP
1.000 0.080 3 188415730 intron variant A/G;T snv 2