Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10033900
CFI
0.807 0.040 4 109737911 intron variant T/C snv 0.54 5
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 5
rs3138141
RDH5 ; BLOC1S1-RDH5
0.827 0.040 12 55721994 3 prime UTR variant C/A snv 0.19 0.16 5
rs12193446
LAMA2 ; LOC102723409
0.925 0.040 6 129498893 intron variant A/G snv 6.4E-02 3
rs9330813
WNT7B
1.000 0.040 22 45968281 intron variant G/A;C snv 3
rs10089517 0.925 0.040 8 59266162 intergenic variant C/A snv 0.31 2
rs524952 0.827 0.040 15 34713685 intergenic variant T/A snv 0.50 2
rs7744813
KCNQ5
0.925 0.040 6 72933566 intron variant C/A snv 0.66 2
rs17400325
PDE11A ; PDE11A-AS1
1.000 0.040 2 177701185 missense variant T/C snv 3.2E-02 2.8E-02 2
rs10500355
RBFOX1
0.925 0.040 16 7409346 intron variant T/A snv 0.29 2
rs9747347
TSPAN10 ; NPLOC4
1.000 0.040 17 81639794 intron variant T/A;C;G snv 2
rs10453441
WNT7B
1.000 0.040 22 45967859 intron variant A/G snv 0.40 2
rs10034228 0.882 0.040 4 111690594 intergenic variant T/C snv 0.32 1
rs10113215 1.000 0.040 8 59219635 intergenic variant A/G snv 0.33 1
rs10512441 1.000 0.040 17 32912627 regulatory region variant C/T snv 0.21 1
rs11658305 1.000 0.040 17 7526004 intergenic variant A/C;T snv 1
rs1370156 1.000 0.040 15 34692682 intergenic variant G/C snv 0.67 1
rs1556867 1.000 0.040 1 164244449 intergenic variant C/T snv 0.24 1
rs4373767 0.882 0.040 1 219586340 regulatory region variant C/T snv 0.32 1
rs61049169 1.000 0.040 2 146131140 intergenic variant G/A;C snv 1
rs634990 0.827 0.040 15 34713872 intergenic variant T/C snv 0.48 1
rs73157695 1.000 0.040 21 45952033 intergenic variant G/A snv 0.29 1
rs9585327 1.000 0.040 13 100037100 intergenic variant G/A snv 0.36 1
rs7162310
APH1B
1.000 0.040 15 63279035 intron variant C/T snv 0.28 1
rs4948523
BICC1
1.000 0.040 10 58579338 intron variant A/C snv 0.51 1