Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs62324212
IL21-AS1
0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 15
rs7705526
TERT
0.776 0.240 5 1285859 intron variant C/A;T snv 15
rs7137828
ATXN2
0.763 0.200 12 111494996 intron variant C/A;T snv 14
rs7831697 0.724 0.240 8 137124061 regulatory region variant T/A;C;G snv 14
rs2738774 0.724 0.240 20 63637985 downstream gene variant G/A;C snv 14
rs11145763
CARD9
0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs10988542
FNBP1
0.724 0.240 9 129894985 intron variant G/A;C snv 14
rs7660520 0.724 0.240 4 182824168 upstream gene variant G/A;C snv 14
rs11580078
C1orf141 ; IL23R
0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
rs55705316 0.724 0.240 1 206760172 regulatory region variant T/A;G snv 14
rs1332099 0.724 0.240 10 99538694 downstream gene variant T/C;G snv 14
rs4869313
ERAP2 ; ERAP1
0.724 0.240 5 96888176 intron variant T/A;G snv 14
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 14
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 13
rs174594
FADS2
0.776 0.160 11 61852357 intron variant C/A;T snv 13
rs4246215
FADS2 ; FEN1
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 13
rs3123543
ATF3
1 212617344 intron variant T/A;C snv 13
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs3840870
COL1A1
17 50184820 3 prime UTR variant -/CTTG delins 13
rs9470361 0.776 0.080 6 36655602 regulatory region variant G/A;T snv 12