Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6986151 1.000 0.040 8 100507673 downstream gene variant T/C snv 0.20 1
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs59185885
IL1RL1 ; IL18R1
1.000 0.040 2 102327786 intron variant T/G snv 0.18 2
rs230504
NFKB1
1.000 0.040 4 102560404 intron variant T/C snv 0.69 1
rs7899004
SUFU
1.000 0.040 10 102581678 intron variant T/C snv 0.44 1
rs12886625 1.000 0.040 14 102772597 intron variant C/G snv 0.38 1
rs2569702
ICAM5
1.000 0.040 19 10293271 intron variant T/C snv 0.39 0.31 1
rs709498 1.000 0.040 3 107975987 regulatory region variant A/G;T snv 1
rs3853750 0.882 0.160 5 110818610 intergenic variant T/C snv 0.30 3
rs111267073 1.000 0.040 5 111030094 intergenic variant C/T snv 1.9E-02 1
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 8
rs3806933
TSLP
0.807 0.360 5 111071044 5 prime UTR variant C/A;T snv 0.40 1
rs1898671
TSLP
0.851 0.160 5 111072304 intron variant C/T snv 0.25 2
rs6594499 0.882 0.120 5 111134439 downstream gene variant C/A snv 0.56 4
rs35441874
CLEC16A
0.882 0.120 16 11119164 intron variant T/A snv 0.19 3
rs62162286
SOCAR ; MIR4435-2HG
1.000 0.040 2 111510863 non coding transcript exon variant A/C;G snv 1
rs11213941 1.000 0.040 11 111563369 downstream gene variant T/C snv 0.35 1
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs1448190
ANAPC1 ; LOC107985933
1.000 0.040 2 111618386 intron variant A/C snv 0.68 1
rs77804393
RMI2 ; LOC105371082
1.000 0.040 16 11265296 intron variant G/A;T snv 1
rs12634229 0.882 0.120 3 112657461 intergenic variant T/C snv 0.15 1
rs13323006 1.000 0.040 3 112904703 regulatory region variant A/G snv 0.31 1
rs2723197 1.000 0.040 2 112932170 upstream gene variant G/A snv 0.36 1
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs12365699 0.882 0.120 11 118872577 regulatory region variant G/A snv 0.12 5