Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs3025039
VEGFA
0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs1982073
TGFB1
0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs12976445
SPACA6 ; SPACA6P-AS ; MIRLET7E ; MIR125A
0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45 20
rs2868371
HSPB1
0.827 0.120 7 76301442 upstream gene variant C/G snv 0.22 6
rs3757
DGCR8 ; TRMT2A
0.851 0.160 22 20111808 3 prime UTR variant G/A snv 0.21 5
rs587782477
APC
0.882 0.120 5 112775679 missense variant A/T snv 4
rs1217371203
CD86
0.882 0.120 3 122106342 missense variant A/G;T snv 4.0E-06; 4.0E-06 4
rs1061285
SMO
0.925 0.120 7 129213467 3 prime UTR variant C/A;G snv 2
rs1633445
TRMT2A
0.925 0.120 22 20113073 non coding transcript exon variant T/A;C snv 1.2E-05; 0.23 2
rs720014
DGCR8
1.000 0.080 22 20111359 3 prime UTR variant T/C snv 0.22 1