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
rs7775
FRZB
0.732 0.240 2 182834857 missense variant G/A;C;T snv 8.0E-05; 8.0E-02; 5.6E-05 14
rs1341239
PRL ; CASC15
0.776 0.360 6 22303975 intron variant A/C snv 0.65 8
rs2287074
MMP2
0.851 0.120 16 55493201 synonymous variant G/A;C snv 0.39; 8.0E-06 4
rs1784418
MMP20 ; LOC101928477
0.851 0.080 11 102613665 intron variant C/A;T snv 0.41 4
rs4970957
MIR554 ; TUFT1
0.925 0.040 1 151544912 intron variant A/G snv 0.16 2
rs5997096
TFIP11
0.925 0.040 22 26499991 intron variant T/C snv 0.47 2
rs2242070
FRZB
1.000 0.040 2 182842127 intron variant G/A snv 0.25 1
rs9288087
FRZB
1.000 0.040 2 182867309 upstream gene variant G/A snv 0.21 1
rs11968525
LOC105378085
1.000 0.040 6 159604175 intron variant G/A snv 0.24 1