Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1212415280
VEGFA
6 43771130 missense variant G/T snv 2.1E-05 2
rs140461341
VEGFA
6 43782078 missense variant G/A snv 3.6E-05 4.2E-05 2
rs1201894677
VEGFA
6 43770833 missense variant G/A snv 1.6E-05 1
rs1421145908
VEGFA
6 43777618 missense variant G/A snv 7.0E-06 1
rs3025010
VEGFA
6 43779840 non coding transcript exon variant T/C;G 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
rs774265827
VEGFA
6 43780773 missense variant G/A;T snv 8.0E-06; 2.0E-05 1
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
rs1222213359
VEGFA
0.574 0.720 6 43770966 missense variant G/A snv 62
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
rs25648
VEGFA
0.742 0.320 6 43771240 synonymous variant C/G;T snv 8.5E-06; 0.16 11
rs2146323
VEGFA
0.752 0.480 6 43777358 non coding transcript exon variant C/A snv 0.31 13
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
rs1287276985
VEGFA
0.790 0.200 6 43782020 missense variant T/A;C snv 4.0E-06; 4.0E-06 7.0E-06 7
rs3025033
VEGFA
0.807 0.360 6 43783338 non coding transcript exon variant A/G snv 0.18 6
rs752907384
VEGFA
0.827 0.200 6 43782077 missense variant C/G;T snv 8.0E-06 6
rs1005230
VEGFA
0.827 0.040 6 43768759 upstream gene variant T/C snv 0.60 5