Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1004446
IGF2 ; INS-IGF2 ; IGF2-AS
0.827 0.240 11 2148913 intron variant G/A snv 0.37 1
rs1015166
TAP2
0.925 0.120 6 32830954 intron variant C/G;T snv 0.28 2
rs10181656
STAT4
0.763 0.360 2 191105153 intron variant G/C snv 0.79 1
rs10277986 1.000 0.120 7 50961290 intron variant T/A;C snv 1
rs1048990
PSMA6
0.790 0.280 14 35292469 5 prime UTR variant C/G;T snv 0.19; 4.0E-06 1
rs1050152
SLC22A4 ; MIR3936HG
0.776 0.480 5 132340627 missense variant C/T snv 0.29 0.28 1
rs10509540
LOC101929727 ; RNLS
0.925 0.160 10 88263276 upstream gene variant T/C snv 0.25 1
rs10517086
LINC02357
0.882 0.160 4 26083889 intron variant G/A snv 0.27 1
rs1052553
MAPT
0.827 0.200 17 45996523 synonymous variant A/G snv 0.14 0.15 1
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 2
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 3
rs10758593
GLIS3
0.827 0.240 9 4292083 intron variant G/A snv 0.45 1
rs10786436
HPSE2
1.000 0.120 10 98540425 intron variant C/T snv 0.40 1
rs10795791 0.925 0.200 10 6066377 upstream gene variant A/G snv 0.40 2
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 3
rs10822050 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 14
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 2
rs10988542
FNBP1
0.724 0.240 9 129894985 intron variant G/A;C snv 14
rs11052552
LINC02390
1.000 0.120 12 9703362 upstream gene variant T/G snv 0.42 1
rs11145763
CARD9
0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs11154178
LOC105377982 ; TRDN
0.807 0.240 6 123540174 intron variant T/A;C snv 7
rs11170445 1.000 0.120 12 53151908 upstream gene variant C/T snv 0.33 1
rs11171739
ERBB3
0.807 0.320 12 56076841 5 prime UTR variant C/T snv 0.49 4
rs11203202
UBASH3A
1.000 0.120 21 42405248 intron variant C/G;T snv 1
rs11203203
UBASH3A
0.807 0.240 21 42416077 intron variant G/A snv 0.28 4