Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 10
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 8
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 6
rs1052553
MAPT
0.827 0.200 17 45996523 synonymous variant A/G snv 0.14 0.15 2
rs1983167 1.000 0.080 X 42989135 regulatory region variant T/C snv 1
rs6494696 1.000 0.080 15 67810868 downstream gene variant G/A;C snv 1
rs6747972 1.000 0.080 2 67843093 intergenic variant A/G snv 0.65 1
rs7881785 1.000 0.080 X 42995357 upstream gene variant A/G snv 1
rs3923809
BTBD9
1.000 0.080 6 38473194 intron variant A/G snv 0.32 1
rs4236060
BTBD9
1.000 0.080 6 38502311 intron variant C/T snv 0.22 1
rs4714156
BTBD9
0.925 0.120 6 38393336 intron variant C/T snv 0.36 1
rs6904723
BTBD9
1.000 0.080 6 38468541 intron variant A/C;T snv 1
rs6923737
BTBD9
1.000 0.080 6 38515788 intron variant T/C snv 0.28 1
rs9296249
BTBD9
0.882 0.120 6 38398065 intron variant T/C snv 0.30 1
rs9357271
BTBD9
0.776 0.160 6 38398097 intron variant T/C snv 0.38 1
rs3104767
CASC16
0.925 0.080 16 52590826 intron variant G/T snv 0.49 1
rs1026732
MAP2K5
1.000 0.080 15 67802747 intron variant G/A snv 0.38 1
rs11635424
MAP2K5
1.000 0.080 15 67745240 intron variant A/G snv 0.53 1
rs12593813
MAP2K5
1.000 0.080 15 67744514 intron variant A/G snv 0.53 1
rs3784709
MAP2K5
1.000 0.080 15 67779937 intron variant C/T snv 0.36 1
rs4489954
MAP2K5
1.000 0.080 15 67779737 intron variant T/A;G snv 1
rs12469063
MEIS1
0.925 0.080 2 66537176 intron variant A/G snv 0.18 1
rs2300478
MEIS1
0.851 0.120 2 66554321 intron variant T/G snv 0.21 1
rs1975197
PTPRD
1.000 0.080 9 8846955 intron variant G/A snv 0.16 1