Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20 8
rs72755233
ADAMTS17
1.000 0.080 15 100152748 missense variant G/A;T snv 7.1E-02; 3.2E-05 5
rs62621197
ADAMTS10
1.000 0.080 19 8605262 missense variant C/A;T snv 4.1E-06; 3.1E-02 2.9E-02 4
rs4678145
UMPS ; MIR544B
0.925 0.120 3 124731234 intron variant G/A;C snv 0.10 2
rs1025128 1.000 0.080 2 59948340 intron variant G/A;C snv 1
rs12406439 1.000 0.080 1 102774795 intron variant C/T snv 0.50 1
rs1863190 1.000 0.080 2 217263429 non coding transcript exon variant A/T snv 0.53 1
rs62422907 1.000 0.080 6 85006237 regulatory region variant G/A snv 8.1E-02 1
rs847139 1.000 0.080 2 176035543 intergenic variant C/T snv 0.15 1
rs55841377
AEBP1
1.000 0.080 7 44105579 intron variant C/A;G snv 1
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 1
rs3828889
HCG26 ; HCP5
1.000 0.080 6 31472874 intron variant T/C snv 0.79 1
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 1
rs6843953
LOC105374494
1.000 0.080 4 13220123 intergenic variant C/T snv 0.14 1
rs6977081
LOC105375567 ; AOC1
1.000 0.080 7 150845427 intron variant G/T snv 0.44 1
rs12104955
LTBP1
1.000 0.080 2 33188236 intron variant C/A;T snv 1
rs486055
MMP10 ; WTAPP1
0.925 0.120 11 102779693 missense variant C/G;T snv 1.2E-05; 0.10 1
rs1866745
SMAD6
1.000 0.080 15 66742474 intron variant G/A snv 0.41 1
rs72725608
TTLL5
1.000 0.080 14 75779563 intron variant T/C snv 3.5E-02 2.6E-02 1