Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1005230
VEGFA
0.827 0.040 6 43768759 upstream gene variant T/C snv 0.60 5
rs10434
VEGFA
0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 17
rs1188254133
VEGFA
0.851 0.240 6 43781990 missense variant T/G snv 7.0E-06 4
rs1201894677
VEGFA
6 43770833 missense variant G/A snv 1.6E-05 1
rs1212415280
VEGFA
6 43771130 missense variant G/T snv 2.1E-05 2
rs1222213359
VEGFA
0.574 0.720 6 43770966 missense variant G/A snv 62
rs1229919945
VEGFA
1.000 0.040 6 43782041 missense variant T/C snv 1
rs1243046808
VEGFA
0.925 0.160 6 43770758 missense variant C/G;T snv 2.0E-05; 9.8E-06 2
rs1284410244
VEGFA
0.925 0.040 6 43778482 missense variant A/G snv 7.0E-06 4
rs1287276985
VEGFA
0.790 0.200 6 43782020 missense variant T/A;C snv 4.0E-06; 4.0E-06 7.0E-06 7
rs1305315912
VEGFA
1.000 0.080 6 43770736 synonymous variant C/T snv 2
rs13207351
VEGFA
0.851 0.280 6 43770057 upstream gene variant A/G;T snv 4
rs1346131223
VEGFA
1.000 6 43777657 missense variant A/G snv 7.4E-06 1
rs1365501228
VEGFA
1.000 0.080 6 43770732 missense variant C/T snv 1.4E-05 2
rs138551969
VEGFA
1.000 0.040 6 43780749 missense variant A/G snv 1.2E-05 3.5E-05 4
rs1404013760
VEGFA
1.000 0.040 6 43771137 missense variant G/C snv 8.9E-06 1
rs140461341
VEGFA
6 43782078 missense variant G/A snv 3.6E-05 4.2E-05 2
rs141138308
VEGFA
1.000 0.040 6 43780784 missense variant C/A;T snv 4.0E-06; 2.8E-05 1
rs1413711
VEGFA
0.882 0.200 6 43772941 intron variant T/A;C snv 3
rs1421145908
VEGFA
6 43777618 missense variant G/A snv 7.0E-06 1
rs1443465532
VEGFA
0.882 0.080 6 43774362 missense variant G/C snv 4.0E-06 7.0E-06 6
rs1479430148
VEGFA
1.000 0.120 6 43784861 3 prime UTR variant A/T snv 1
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs2146323
VEGFA
0.752 0.480 6 43777358 non coding transcript exon variant C/A snv 0.31 13