Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1201894677
VEGFA
6 43770833 missense variant G/A snv 1.6E-05 1
rs1229919945
VEGFA
1.000 0.040 6 43782041 missense variant T/C snv 1
rs1346131223
VEGFA
1.000 6 43777657 missense variant A/G snv 7.4E-06 1
rs1404013760
VEGFA
1.000 0.040 6 43771137 missense variant G/C snv 8.9E-06 1
rs141138308
VEGFA
1.000 0.040 6 43780784 missense variant C/A;T snv 4.0E-06; 2.8E-05 1
rs1421145908
VEGFA
6 43777618 missense variant G/A snv 7.0E-06 1
rs1479430148
VEGFA
1.000 0.120 6 43784861 3 prime UTR variant A/T snv 1
rs3025000
VEGFA
1.000 0.120 6 43778432 non coding transcript exon variant C/T snv 0.29 0.23 1
rs3025010
VEGFA
6 43779840 non coding transcript exon variant T/C;G snv 1
rs3025036
VEGFA
1.000 0.080 6 43783932 non coding transcript exon variant G/A;C;T snv 1
rs376388064
VEGFA
6 43782006 missense variant C/T snv 2.8E-05 3.5E-05 1
rs541717889
VEGFA
6 43770888 missense variant G/C snv 2.1E-05 1
rs554561071
VEGFA
6 43777513 missense variant A/G snv 1.2E-05 3.5E-05 1
rs735286
VEGFA
6 43776884 non coding transcript exon variant C/T snv 0.23 1
rs749491856
VEGFA
1.000 6 43782071 missense variant A/C snv 1
rs774265827
VEGFA
6 43780773 missense variant G/A;T snv 8.0E-06; 2.0E-05 1
rs1212415280
VEGFA
6 43771130 missense variant G/T snv 2.1E-05 2
rs1243046808
VEGFA
0.925 0.160 6 43770758 missense variant C/G;T snv 2.0E-05; 9.8E-06 2
rs1305315912
VEGFA
1.000 0.080 6 43770736 synonymous variant C/T snv 2
rs1365501228
VEGFA
1.000 0.080 6 43770732 missense variant C/T snv 1.4E-05 2
rs140461341
VEGFA
6 43782078 missense variant G/A snv 3.6E-05 4.2E-05 2
rs3025053
VEGFA
0.925 0.120 6 43785588 3 prime UTR variant G/A snv 8.6E-02 2
rs748352475
VEGFA
0.925 0.160 6 43777546 missense variant C/G snv 1.2E-05 7.0E-06 2
rs748984440
VEGFA
1.000 0.040 6 43784546 stop lost A/C snv 4.0E-06 2
rs766474822
VEGFA
0.925 0.080 6 43770990 missense variant G/A snv 1.4E-05 2.1E-05 2