Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35489971
CD300LF ; RAB37
1.000 0.040 17 74704804 missense variant A/G;T snv 0.73 2
rs1521516
DIP2B
12 50661925 intron variant C/T snv 0.27 2
rs6054
FGB
1.000 0.080 4 154568456 missense variant C/T snv 2.4E-03 2.7E-03 2
rs148685782
FGG
1.000 0.080 4 154611883 missense variant G/C snv 1.9E-03 2.2E-03 2
rs10489615
GALNT2
1 230169242 intron variant A/C;G snv 2
rs11102001
GSTM5 ; EPS8L3
0.925 0.080 1 109757069 missense variant G/A snv 9.4E-02 0.16 2
rs16844401
HGFAC
1.000 0.040 4 3447925 missense variant G/A;T snv 7.5E-02; 8.3E-06 2
rs2522056
IRF1-AS1
5 132466034 intron variant G/A snv 0.25 2
rs11780978
PLEC
1.000 0.040 8 143960684 intron variant G/A snv 0.30 2
rs10512597
RAB37 ; CD300LF
17 74703694 intron variant T/A;C snv 2
rs3091307
TH2LCRR
0.925 0.160 5 132653444 intron variant A/G snv 0.34 2
rs10226084 7 17957989 upstream gene variant T/C snv 0.46 1
rs12511469 4 154530607 downstream gene variant T/A snv 0.18 1
rs12699921 7 17954871 intergenic variant G/A snv 0.40 1
rs1938492 1 65652146 intergenic variant A/C snv 0.43 1
rs194714 14 68828731 intergenic variant T/C snv 0.24 1
rs194741 14 68821715 intergenic variant A/G snv 0.24 1
rs2376015 1 65658091 intergenic variant A/G snv 0.43 1
rs2420915 10 121080764 regulatory region variant G/A snv 0.25 1
rs367677 14 68806373 intergenic variant A/G snv 0.25 1
rs434943 14 68847342 intergenic variant G/A snv 0.27 1
rs4655582 1 65687680 regulatory region variant C/G snv 0.34 1
rs4817986 21 39093586 regulatory region variant G/T snv 0.22 1
rs511154 3 136232079 intergenic variant A/G;T snv 1
rs6010044 22 50663510 intergenic variant A/C snv 0.20 1