Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2239527 1.000 0.080 6 31542002 5 prime UTR variant C/G snv 0.33 0.38 1
rs6011456 1.000 0.080 20 62899372 intron variant T/A;G snv 1
rs2477786 1.000 0.080 1 65266559 intron variant C/T snv 0.20 1
rs10263017 1.000 0.080 7 6026173 intron variant G/C;T snv 1
rs301164 1.000 0.080 16 85780274 non coding transcript exon variant T/A;C snv 1
rs2339745 1.000 0.080 5 172933031 non coding transcript exon variant G/A;C;T snv 1
rs778747981
F2R
1.000 0.080 5 76732556 missense variant G/A snv 8.0E-06 7.0E-06 1
rs3354
F3
1.000 0.080 1 94530263 3 prime UTR variant C/A;G;T snv 0.28 1
rs774688955
F3
1.000 0.080 1 94541666 5 prime UTR variant G/A;T snv 1
rs11666735 1.000 0.080 19 54885501 missense variant G/A snv 6.9E-02 6.6E-02 1
rs370102050 1.000 0.080 19 54889671 missense variant G/A snv 3.6E-05 1.0E-04 1
rs1800791
FGB
1.000 0.080 4 154562157 upstream gene variant G/A snv 0.15 1
rs1049636
FGG
1.000 0.080 4 154604818 3 prime UTR variant G/A snv 0.67 0.70 1
rs781888882 1.000 0.080 1 147908067 missense variant G/A snv 4.0E-06 1
rs750278262 1.000 0.080 17 4934537 missense variant A/G snv 4.0E-06 1
rs2243093 1.000 0.080 17 4932600 splice region variant T/C snv 0.16 0.17 1
rs2774052 1.000 0.080 14 59433302 intron variant A/G snv 0.47 1
rs6804193 1.000 0.080 3 170064416 intron variant T/C snv 0.44 1
rs12118721 1.000 0.080 1 154424940 intron variant T/C snv 0.51 1
rs938043469 1.000 0.080 5 53051452 synonymous variant T/C snv 7.0E-06 1
rs2286797 1.000 0.080 3 52795617 synonymous variant G/A snv 4.5E-02 1.7E-02 1
rs2295394 1.000 0.080 14 92946398 synonymous variant G/A snv 8.4E-02 7.3E-02 1
rs2075624
IVD
1.000 0.080 15 40418524 3 prime UTR variant G/A snv 0.24 1
rs2562059 1.000 0.080 16 87605249 intron variant C/G snv 0.51 1
rs2306799 1.000 0.080 19 43769889 intron variant G/A;T snv 1