Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs3025039
VEGFA
0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs10434
VEGFA
0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 17
rs2146323
VEGFA
0.752 0.480 6 43777358 non coding transcript exon variant C/A snv 0.31 13
rs833069
VEGFA
0.851 0.200 6 43774842 non coding transcript exon variant T/C;G snv 5
rs13207351
VEGFA
0.851 0.280 6 43770057 upstream gene variant A/G;T snv 4
rs3025021
VEGFA
0.882 0.160 6 43781426 non coding transcript exon variant T/C snv 0.70 4
rs1243046808
VEGFA
0.925 0.160 6 43770758 missense variant C/G;T snv 2.0E-05; 9.8E-06 2
rs748352475
VEGFA
0.925 0.160 6 43777546 missense variant C/G snv 1.2E-05 7.0E-06 2