Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs679620
MMP3
0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 17
rs2252070
MMP13
0.752 0.320 11 102955810 upstream gene variant C/T snv 0.68 13
rs11225395
MMP8
0.776 0.360 11 102725749 intron variant A/C;G snv 11
rs587778430
KDR
0.807 0.280 4 55110466 missense variant C/T snv 1.2E-05 7.0E-06 7
rs12722
COL5A1 ; LOC101448202
0.882 0.120 9 134842570 3 prime UTR variant C/T snv 0.44 6
rs650108
MMP3
0.827 0.160 11 102838056 intron variant G/A snv 0.31 6
rs1144393
MMP1 ; WTAPP1
0.851 0.160 11 102798678 intron variant T/C snv 0.30 5
rs3196378
LOC101448202 ; COL5A1
0.882 0.080 9 134843036 3 prime UTR variant C/A;G;T snv 4
rs11154027 1.000 0.080 6 121460244 intergenic variant T/C snv 0.61 3
rs2761884
BMP4
0.925 0.120 14 53954334 intron variant G/T snv 0.34 3
rs900379
FGF10
1.000 0.080 5 44369554 intron variant C/T snv 0.53 2
rs9505888
THBS2 ; LOC101929523
1.000 0.080 6 169225779 intron variant A/G snv 0.57 2
rs4362400
VAT1L ; LOC105371351
1.000 0.080 16 77939459 intron variant A/C;G snv 0.49 2