Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs1005230
VEGFA
0.827 0.040 6 43768759 upstream gene variant T/C snv 0.60 5
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs13207351
VEGFA
0.851 0.280 6 43770057 upstream gene variant A/G;T snv 4
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
rs1365501228
VEGFA
1.000 0.080 6 43770732 missense variant C/T snv 1.4E-05 2
rs1305315912
VEGFA
1.000 0.080 6 43770736 synonymous variant C/T snv 2
rs1243046808
VEGFA
0.925 0.160 6 43770758 missense variant C/G;T snv 2.0E-05; 9.8E-06 2
rs914956206
VEGFA
0.882 0.080 6 43770762 missense variant G/A;T snv 4
rs1201894677
VEGFA
6 43770833 missense variant G/A snv 1.6E-05 1
rs541717889
VEGFA
6 43770888 missense variant G/C snv 2.1E-05 1
rs1222213359
VEGFA
0.574 0.720 6 43770966 missense variant G/A snv 62
rs766474822
VEGFA
0.925 0.080 6 43770990 missense variant G/A snv 1.4E-05 2.1E-05 2
rs1212415280
VEGFA
6 43771130 missense variant G/T snv 2.1E-05 2
rs1404013760
VEGFA
1.000 0.040 6 43771137 missense variant G/C snv 8.9E-06 1
rs25648
VEGFA
0.742 0.320 6 43771240 synonymous variant C/G;T snv 8.5E-06; 0.16 11
rs1413711
VEGFA
0.882 0.200 6 43772941 intron variant T/A;C snv 3
rs1443465532
VEGFA
0.882 0.080 6 43774362 missense variant G/C snv 4.0E-06 7.0E-06 6
rs833068
VEGFA
0.851 0.120 6 43774790 non coding transcript exon variant G/A snv 0.36 4
rs833069
VEGFA
0.851 0.200 6 43774842 non coding transcript exon variant T/C;G snv 5
rs833070
VEGFA
0.776 0.440 6 43774889 non coding transcript exon variant T/C snv 0.58 11
rs3024994
VEGFA
0.776 0.120 6 43775770 non coding transcript exon variant C/T snv 3.8E-02 8
rs735286
VEGFA
6 43776884 non coding transcript exon variant C/T snv 0.23 1
rs2146323
VEGFA
0.752 0.480 6 43777358 non coding transcript exon variant C/A snv 0.31 13