Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5967638 0.925 0.040 X 85840734 downstream gene variant G/A snv 0.16 2
rs2046315
LOC105375631
0.925 0.040 8 89198871 intergenic variant A/G snv 0.71 2
rs16954776 1.000 0.040 13 98048363 intergenic variant A/G snv 0.12 1
rs723794 1.000 0.040 4 145954399 downstream gene variant G/T snv 0.64 1
rs6818964
ANKRD17
1.000 0.040 4 73104747 intron variant C/G;T snv 1
rs11134654
GABRP
1.000 0.040 5 170813419 3 prime UTR variant A/C snv 0.81 1
rs17826057
IRAK3
1.000 0.040 12 66239384 intron variant G/A snv 8.6E-02 1
rs1064524
ITGAL
1.000 0.040 16 30481502 missense variant C/T snv 3.3E-02 3.3E-02 1
rs1488864
LOC101927825 ; CAVIN3
0.851 0.080 11 6321099 intron variant T/G snv 0.80 1
rs9471075
LOC105375047 ; KIF6
1.000 0.040 6 39339256 intron variant A/C snv 0.14 1
rs16867579
NACA4P
1.000 0.040 8 101363039 intron variant A/C snv 0.11 1
rs17111530
TSHR ; LOC101928462
1.000 0.040 14 81132568 intron variant T/C snv 0.16 1