Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs3804099
TLR2
0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs3804100
TLR2
0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs1982073
TGFB1
0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs2981573
IL20
0.882 0.160 1 206867232 intron variant G/A snv 0.77 4
rs2243158
IL19
0.925 0.120 1 206834296 5 prime UTR variant C/A;G;T snv 2
rs2981572
IL20
1.000 0.080 1 206864800 upstream gene variant G/T snv 0.53 1