Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 23
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 13
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 9
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 8
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 7
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 7
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 6
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 6
rs8176746
ABO
0.882 0.160 9 133255935 missense variant G/A;T snv 4.1E-06; 0.12 6
rs10184428 2 164155317 intron variant C/A;G snv 5
rs11099098 0.925 0.120 4 80248758 intergenic variant G/C;T snv 5
rs13149993 4 80237391 regulatory region variant G/A;C snv 5
rs167479
RGL3
19 11416089 missense variant T/A;C;G snv 5
rs17514846
FURIN
0.882 0.120 15 90873320 intron variant C/A;G snv 5
rs2067087
HOTTIP ; HOXA13
1.000 0.080 7 27202041 non coding transcript exon variant G/C;T snv 5
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 4
rs1126464
DPEP1
1.000 0.040 16 89637957 missense variant G/A;C snv 1.3E-05; 0.26 4
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 4
rs1859168
HOTTIP
0.790 0.160 7 27202740 non coding transcript exon variant A/C;G;T snv 4
rs2274700
CFH
0.776 0.240 1 196713817 synonymous variant G/A;C;T snv 0.44 4
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 4
rs62524579 8 142979538 downstream gene variant G/A;C;T snv 4
rs6418
GML ; CYP11B2
8 142914947 intron variant A/C;G snv 0.42 4