Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 12
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 10
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 9
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 9
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 7
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 6
rs3217992
CDKN2B-AS1 ; CDKN2B
0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32 6
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 5
rs2206734
CDKAL1
0.882 0.160 6 20694653 intron variant C/T snv 0.20 3
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 3
rs12413624 0.851 0.120 10 118519432 intergenic variant T/A snv 0.34 2
rs7503953 0.882 0.320 17 6238357 intergenic variant A/C snv 0.81 2
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 2
rs9543325 0.882 0.200 13 73342491 regulatory region variant C/G;T snv 2
rs2236479
COL18A1 ; SLC19A1
0.925 0.160 21 45499218 intron variant G/A snv 0.40 2
rs2941471
HNF4G
0.851 0.240 8 75558169 intron variant G/A snv 0.65 2
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 2
rs1455311
LINC01088
0.925 0.160 4 79043433 intron variant A/G snv 0.14 2
rs1810636
LOC105372507
0.925 0.160 20 2674279 regulatory region variant A/C;T snv 2
rs3790844
NR5A2
0.882 0.200 1 200038304 intron variant A/C;G snv 2