Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs511154 3 136232079 intergenic variant A/G;T snv 3
rs6010044 22 50663510 intergenic variant A/C snv 0.20 3
rs743562 5 132536691 intron variant C/T snv 0.35 3
rs7673587 4 154559282 upstream gene variant C/T snv 0.24 3
rs7204230
CHD9
16 53158419 intron variant T/C snv 0.31 3
rs715
CPS1
1.000 0.040 2 210678331 3 prime UTR variant T/C snv 0.28 3
rs12651106
DCHS2
4 154379907 intron variant C/A snv 0.12 3
rs7968440
DIP2B
12 50740958 intron variant A/G snv 0.28 3
rs1476698
FARP2
2 241357034 intron variant A/G;T snv 3
rs2070016
FGA
1.000 0.040 4 154589162 intron variant A/G snv 0.12 3
rs1800787
FGB
1.000 0.040 4 154562863 upstream gene variant C/T snv 0.17 3
rs1800788
FGB
4 154562762 upstream gene variant C/T snv 0.18 3
rs1800789
FGB
1.000 0.040 4 154561591 upstream gene variant G/A snv 0.17 3
rs1800790
FGB
0.851 0.200 4 154562556 upstream gene variant G/A snv 0.15 3
rs2059503
FGB
4 154572267 downstream gene variant A/T snv 0.14 3
rs2227421
FGB
4 154571072 3 prime UTR variant A/C snv 0.26 3
rs4220
FGB
0.925 0.080 4 154570607 missense variant G/A snv 0.17 0.15 3
rs6054
FGB
1.000 0.080 4 154568456 missense variant C/T snv 2.4E-03 2.7E-03 3
rs6056
FGB
4 154567669 synonymous variant C/T snv 0.17 0.15 3
rs6058
FGB
4 154569192 synonymous variant G/T snv 5.2E-03 2.1E-02 3
rs16844401
HGFAC
1.000 0.040 4 3447925 missense variant G/A;T snv 7.5E-02; 8.3E-06 3
rs12712127
IL1R1
2 102110201 intron variant A/G snv 0.62 3
rs2106854
IRF1-AS1
5 132433482 intron variant C/T snv 0.23 3
rs2522056
IRF1-AS1
5 132466034 intron variant G/A snv 0.25 3
rs6874639
IRF1-AS1
5 132443024 intron variant A/G snv 0.24 3