Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3755955
IDUA
0.925 0.080 4 1000626 missense variant G/A;C snv 0.16; 8.0E-06 1
rs6831280
IDUA
0.925 0.080 4 1002377 missense variant G/A;C snv 0.17 1
rs6827815 4 1005657 upstream gene variant C/A;G snv 1
rs6866306 5 100650833 downstream gene variant T/C snv 0.39 1
rs76051363
FGFRL1
4 1013199 intron variant C/G;T snv 1
rs56396408
FGFRL1
4 1014598 intron variant C/T snv 0.12 1
rs2273061
JAG1
1.000 0.080 20 10658895 intron variant G/A snv 0.46 1
rs3790160
JAG1
20 10659340 intron variant T/C snv 0.54 1
rs6040063
JAG1
20 10660229 intron variant A/G snv 0.54 1
rs6539288 12 106904084 upstream gene variant A/T snv 0.63 1
rs1037011 12 106909000 upstream gene variant T/C snv 0.64 1
rs7548588 1 109933349 downstream gene variant T/C snv 0.36 1
rs7364724 1 109937598 intergenic variant A/G;T snv 1
rs73349318
LOC105378481
10 110485642 intron variant A/T snv 9.7E-02 1
rs818427
SRP19 ; REEP5
5 112886172 intron variant C/T snv 0.29 1
rs73200209
MED13L
12 116117981 intron variant A/C;T snv 0.17 1
rs1878526 2 118281022 intergenic variant G/A snv 0.24 1
rs148285156 2 118577128 intergenic variant A/G snv 7.1E-03 1
rs115242848 2 118750031 intergenic variant C/T snv 7.5E-03 1
rs55983207
LINC01956
2 118772253 intron variant T/C snv 2.9E-02 1
rs144832051 2 118852830 intergenic variant C/T snv 1.3E-02 1
rs12612325 2 118874676 intergenic variant G/A snv 0.26 1
rs4355801 0.882 0.120 8 118911634 regulatory region variant A/G;T snv 1
rs7010267
TNFRSF11B
8 118934417 intron variant C/A snv 0.38 1
rs7839059
COLEC10
8 118964303 intergenic variant C/A snv 0.40 1