Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 9
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 8
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 7
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 6
rs11172113
LRP1
0.882 0.080 12 57133500 intron variant T/C snv 0.42 6
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 5
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 4
rs11624776 14 93129246 regulatory region variant A/C;T snv 3
rs7577262 2 233910224 intergenic variant G/A;T snv 3
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 3
rs4810485
CD40
0.732 0.480 20 46119308 intron variant T/A;G snv 3
rs11187838
PLCE1-AS1 ; PLCE1
10 94278929 non coding transcript exon variant G/A snv 0.44 3
rs1024905 1.000 0.040 12 4408974 downstream gene variant G/A;C snv 2
rs12134493 0.925 0.040 1 115135325 TF binding site variant C/A snv 9.2E-02 2
rs2078371 1.000 0.040 1 115134562 regulatory region variant T/C snv 0.14 2
rs1800888
ADRB2
0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 2
rs6478241
ASTN2
0.925 0.040 9 116490350 intron variant A/G;T snv 2
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 2
rs12681792
CLVS1
8 61141904 intron variant C/A snv 0.23 2
rs9486719
FHL5
1.000 0.040 6 96612248 intron variant G/A snv 0.26 2
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs10456100
KCNK5
1.000 0.040 6 39215694 intron variant C/T snv 0.20 2