Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 11
rs1537372
CDKN2B-AS1
0.752 0.120 9 22103184 intron variant G/A;T snv 11
rs2179593
TOX2
0.790 0.080 20 44031646 intron variant C/A snv 0.71 11
rs2738783
RTEL1 ; RTEL1-TNFRSF6B
0.763 0.160 20 63677259 intron variant T/G snv 0.85 11
rs35107139
BMP4
0.776 0.080 14 53952388 intron variant A/C;G;T snv 11
rs35446936
ACTRT3
0.776 0.080 3 169768720 intron variant G/A snv 0.21 11
rs10049390
SLCO2A1
0.776 0.080 3 133982275 intron variant G/A snv 0.67 10
rs10457678
ECT2L
0.790 0.080 6 138801103 intron variant A/G snv 0.19 10
rs10511330
ZBTB20
0.776 0.080 3 114402172 intron variant T/C snv 0.22 10
rs10980628
LPAR1
0.776 0.080 9 110909123 intron variant T/C snv 0.16 10
rs11085466
LOC101929007
0.790 0.080 19 21569009 intron variant G/C snv 0.23 10
rs11150038
CLEC3A
0.790 0.080 16 78042662 intron variant A/C;G snv 10
rs11196170
TCF7L2
0.776 0.080 10 112962862 intron variant G/A;C snv 10
rs117079142
LOC112268030 ; UTP23
0.776 0.080 8 116778675 intron variant C/A snv 3.0E-02 10
rs11874392
SMAD7
0.763 0.080 18 48926786 intron variant A/T snv 0.50 10
rs11884596
LOC105373831
0.776 0.080 2 198747683 intron variant T/C snv 0.32 10
rs12246635
VTI1A
0.776 0.080 10 112528860 intron variant T/C snv 0.13 10
rs12372718
ATF1
0.776 0.080 12 50777307 intron variant A/G snv 0.35 10
rs1250567
ZMIZ1
0.776 0.080 10 79286508 intron variant T/C snv 0.56 10
rs12548629
BAALC ; BAALC-AS1
0.776 0.120 8 103189173 intron variant C/T snv 0.24 10
rs12594720
SMAD6
0.776 0.080 15 66714680 intron variant C/G snv 0.23 10
rs12646351
ZNF827
0.790 0.080 4 145819473 intron variant G/A snv 0.19 10
rs1391441
TET2-AS1 ; TET2
0.763 0.240 4 105207603 intron variant G/A snv 0.70 10
rs145364999
CHD1
0.776 0.080 5 98870378 intron variant T/A snv 1.9E-03 10
rs16878812
LOC112267956 ; FKBP5
0.776 0.080 6 35601785 intron variant A/G snv 0.15 10