Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs2070016
FGA
1.000 0.040 4 154589162 intron variant A/G snv 0.12 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
rs4463047 4 154574381 downstream gene variant T/C snv 0.15 3
rs4508864 4 154560137 upstream gene variant C/G;T snv 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
rs7673587 4 154559282 upstream gene variant C/T snv 0.24 3
rs2073643 1.000 0.080 5 132387596 intron variant T/C snv 0.46 4
rs2158177 0.925 0.120 5 132648366 intron variant A/G snv 0.18 4
rs1016988 5 132408882 upstream gene variant T/C snv 0.20 3
rs11242111 5 132420366 intron variant A/G;T snv 3
rs12777 5 132335969 synonymous variant C/G snv 3.1E-02 2.8E-02 3
rs17690122 5 132532143 intron variant A/G;T snv 3
rs2106854 5 132433482 intron variant C/T snv 0.23 3
rs2522056 5 132466034 intron variant G/A snv 0.25 3
rs270607 5 132313493 intron variant A/G snv 0.69 3
rs3091307 0.925 0.160 5 132653444 intron variant A/G snv 0.34 3
rs6873426 5 132482939 3 prime UTR variant G/T snv 0.38 3
rs6874639 5 132443024 intron variant A/G snv 0.24 3