Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 25
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 21
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 20
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 18
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 17
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 15
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 13
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 11
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 10
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 10
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 9
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 8
rs880315
CASZ1
0.925 0.120 1 10736809 intron variant T/C snv 0.32 8
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 8
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 7
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 7
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 7
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 7