Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs212402
LOC105378083
1.000 0.080 6 159051263 intron variant G/A snv 0.66 3
rs2249937
LOC112267968
1.000 0.080 6 159094277 non coding transcript exon variant T/G snv 0.76 3
rs654690
LOC112267968
1.000 0.080 6 159093746 intron variant T/A;C snv 3
rs6726160
NONOP2
1.000 0.080 2 60937594 non coding transcript exon variant T/G snv 0.47 2
rs1018326
LINC01934
1.000 0.080 2 181143073 intron variant T/C snv 0.47 1
rs10188217
PUS10
0.925 0.080 2 60990407 intron variant T/A;C snv 1
rs1033180 1.000 0.080 6 383546 regulatory region variant C/T snv 5.4E-02 1
rs10796045 1.000 0.080 10 6360779 intergenic variant G/T snv 0.79 1
rs10800746
INAVA
1.000 0.080 1 200912264 intron variant C/T snv 0.32 1
rs10883365
LINC01475
0.882 0.080 10 99528007 non coding transcript exon variant G/A snv 0.52 1
rs10886159 1.000 0.080 10 117854099 intergenic variant T/C snv 0.25 1
rs11711054 1.000 0.080 3 46304120 intergenic variant G/A snv 0.73 1
rs11734090
KIAA1109
1.000 0.080 4 122306958 intron variant T/C snv 0.25 1
rs11851414
ZFP36L1
1.000 0.080 14 68792785 intron variant T/C snv 0.25 1
rs11875687
PTPN2
1.000 0.080 18 12843138 intron variant T/C snv 0.17 1
rs12142280 1.000 0.080 1 172895512 intron variant T/A snv 0.21 1
rs12727642 1.000 0.080 1 7986612 upstream gene variant C/A snv 0.12 1
rs13096142
CCR3
1.000 0.080 3 46240253 intron variant C/T snv 0.25 1
rs1378938 1.000 0.080 15 74804102 downstream gene variant T/A;C snv 1
rs1394220
LOC105377891
1.000 0.080 6 90309585 intron variant A/C snv 0.34 1
rs1468788
SLC9A4
1.000 0.080 2 102476054 intron variant C/T snv 0.54 1
rs169858
LOC105378083 ; LOC112267968
1.000 0.080 6 159063744 intron variant T/C snv 0.76 1
rs182429
LOC107986664 ; LOC105378083
1.000 0.080 6 159048542 intron variant A/G snv 0.49 1
rs1997179 1.000 0.080 4 122063478 intergenic variant T/C snv 0.21 1
rs2097282 1.000 0.080 3 46336534 intergenic variant C/T snv 0.68 1