Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs2285053
MMP2
0.752 0.320 16 55478465 intron variant C/T snv 0.12 15
rs142319636
MMP2
0.790 0.080 16 55504828 intron variant A/G snv 3.7E-02 9
rs243866
MMP2
0.827 0.120 16 55477625 intron variant G/A snv 0.19 8
rs763201736
MMP2
0.807 0.200 16 55498391 missense variant C/T snv 4.0E-06 8
rs1238968510
MMP2
0.882 0.080 16 55479556 missense variant A/G;T snv 4.1E-06 2.1E-05 4
rs2287074
MMP2
0.851 0.120 16 55493201 synonymous variant G/A;C snv 0.39; 8.0E-06 4
rs7201
MMP2
0.925 0.160 16 55505702 3 prime UTR variant A/C snv 0.37 4
rs243864
MMP2
0.925 0.080 16 55478410 intron variant T/G snv 0.19 3
rs11639960
MMP2
0.925 0.080 16 55499358 intron variant A/G snv 0.26 2
rs11643630
MMP2
0.925 0.080 16 55476547 intron variant T/G snv 0.55 2
rs11644561
MMP2
0.925 0.080 16 55475122 intron variant G/A snv 0.20 2
rs121912955
MMP2
0.925 0.200 16 55491830 missense variant G/A snv 2
rs12934241
MMP2
0.925 0.040 16 55486666 non coding transcript exon variant C/G;T snv 2
rs1477017
MMP2
0.925 0.080 16 55483250 intron variant A/G snv 0.38 2
rs17301608
MMP2
0.925 0.080 16 55484698 intron variant C/A;G;T snv 2
rs17859821
MMP2
1.000 0.040 16 55478141 intron variant G/A;C snv 0.11 2
rs755990134
MMP2
0.925 0.080 16 55489730 synonymous variant C/T snv 3.2E-05 7.0E-06 2
rs764664272
MMP2
1.000 0.120 16 55484060 missense variant A/G snv 1.2E-05 7.0E-06 2
rs767232094
MMP2
1.000 0.040 16 55484157 synonymous variant C/T snv 8.0E-06 2
rs1022088103
MMP2
16 55485759 missense variant G/A snv 1
rs1132896
MMP2
16 55485623 synonymous variant G/C snv 0.31 0.26 1
rs11646643
MMP2
1.000 0.040 16 55484965 intron variant A/G snv 0.31 1
rs121912953
MMP2
1.000 0.040 16 55483057 missense variant G/A snv 4.0E-06 1
rs121912954
MMP2
1.000 0.040 16 55485677 stop gained C/A;G snv 1