Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 17
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 11
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 10
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 10
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs514659
ABO
0.882 0.120 9 133266790 intron variant C/A;T snv 8
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 8
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 7
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 7
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 7
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 7
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 7
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 7
rs564398
CDKN2B-AS1
0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 7
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 7
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 7
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 7
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 6