Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12863738 0.724 0.240 X 136949968 intron variant C/T snv 0.16 14
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
rs2664170
GAB3
1.000 0.120 X 154717327 intron variant G/A snv 1
rs5979785 0.925 0.160 X 12953405 intergenic variant C/T snv 1
rs229541
C1QTNF6
0.807 0.200 22 37195278 intron variant G/A snv 0.49 6
rs428595
LOC107985532
1.000 0.120 22 21662102 non coding transcript exon variant A/G snv 0.98 3
rs2281135
PNPLA3
0.851 0.160 22 43936690 intron variant G/A snv 0.19 2
rs229533
C1QTNF6
1.000 0.120 22 37191071 intron variant A/C snv 0.50 1
rs4820830
HORMAD2
1.000 0.120 22 30135102 intron variant C/G;T snv 0.71 1
rs5753037
HORMAD2 ; LOC105372988
0.925 0.160 22 30185733 intron variant C/A;T snv 1
rs2836882 0.724 0.240 21 39094644 intergenic variant G/A snv 0.23 15
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 7
rs11203203
UBASH3A
0.807 0.240 21 42416077 intron variant G/A snv 0.28 4
rs11203202
UBASH3A
1.000 0.120 21 42405248 intron variant C/G;T snv 1
rs3788013
UBASH3A
0.851 0.240 21 42421219 intron variant C/A snv 0.44 1
rs6518350
GATD3A ; LOC107983952
1.000 0.120 21 44201934 non coding transcript exon variant A/G snv 1
rs9976767
UBASH3A
0.882 0.200 21 42416281 intron variant A/G snv 0.45 1
rs2738774 0.724 0.240 20 63637985 downstream gene variant G/A;C snv 14
rs143383
GDF5
0.724 0.320 20 35438203 5 prime UTR variant G/A snv 0.47 2
rs2281808
SIRPG
0.925 0.160 20 1629905 intron variant T/A;C snv 2
rs6043409
SIRPG ; SIRPG-AS1
1.000 0.120 20 1635560 missense variant A/G snv 0.73 0.72 2
rs61734651
COL9A3
0.882 0.280 20 62819980 missense variant C/T snv 4.7E-02 4.5E-02 1
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20
rs602662
LOC105447645 ; FUT2
0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47 15
rs62131887 0.724 0.240 19 10476920 intergenic variant C/T snv 0.37 14