Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 6
rs6659932
IL12RB2
0.827 0.240 1 67336688 intron variant A/C snv 0.81 4
rs1517352
STAT4
0.851 0.160 2 191066738 intron variant A/C snv 0.45 3
rs10498070 0.925 0.080 2 219833404 intergenic variant A/C snv 0.39 2
rs6568431
ATG5
0.790 0.320 6 106140931 intron variant A/C snv 0.61 2
rs7172677 0.925 0.080 15 75132252 intergenic variant A/C snv 0.71 2
rs13280095
PVT1
1.000 0.080 8 128166844 intron variant A/C snv 0.26 1
rs1734787
MECP2
1.000 0.080 X 154059995 non coding transcript exon variant A/C snv 0.17 1
rs180977001
PXK
1.000 0.080 3 58332737 upstream gene variant A/C snv 4.4E-02 1
rs729302 0.827 0.160 7 128928906 intergenic variant A/C snv 0.28 1
rs7300146
GLT1D1
1.000 0.080 12 128888528 intron variant A/C snv 0.23 1
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 7
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 7
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 7
rs12531711
TNPO3
0.827 0.200 7 128977412 intron variant A/C;G snv 5
rs10946940 1.000 0.080 6 27592808 upstream gene variant A/C;G snv 1
rs1194
ZNF76
1.000 0.080 6 35295778 3 prime UTR variant A/C;G snv 0.78 1
rs280519
TYK2
0.752 0.320 19 10362257 splice region variant A/C;G snv 0.50 1
rs9275428 0.925 0.120 6 32703201 downstream gene variant A/C;G snv 1
rs11145763
CARD9
0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs268134
SPRED2
0.925 0.120 2 65381229 intron variant A/C;G;T snv 3
rs601162 0.925 0.160 9 29632144 upstream gene variant A/C;G;T snv 2
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 1
rs3130342
TNXB
1.000 0.080 6 32112369 non coding transcript exon variant A/C;G;T snv 1
rs9394274
TCP11
1.000 0.080 6 35147134 intron variant A/C;G;T snv 1