Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5516
KLK1
0.827 0.120 19 50820217 missense variant C/G snv 0.69 0.67 6
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs4988300
LRP5
0.925 0.120 11 68321363 intron variant G/T snv 0.50 2
rs4916251
DNM3 ; PIGC
0.882 0.040 1 172377256 intron variant T/A snv 0.70 3
rs4898
TIMP1 ; SYN1 ; MIR4769
0.672 0.520 X 47585586 synonymous variant T/C snv 0.46 0.46 25
rs486055
MMP10 ; WTAPP1
0.925 0.120 11 102779693 missense variant C/G;T snv 1.2E-05; 0.10 3
rs3918242
MMP9
0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs3877899
CCDC152 ; SELENOP
0.827 0.160 5 42801166 missense variant C/A;T snv 4.0E-06; 0.20 7
rs3827066
ZNF335
0.925 0.040 20 45957384 intron variant C/T snv 0.12 2
rs3781590
LRP5
1.000 0.040 11 68391684 intron variant G/A snv 0.35 1
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs326118
MTRR ; FASTKD3
0.925 0.080 5 7868430 intron variant T/G snv 0.21 2
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 17
rs3025058
MMP3
0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs3019885
SLC30A8
0.925 0.120 8 117013406 intron variant T/A;G snv 2
rs2836411
ERG
1.000 0.040 21 38447907 intron variant C/A;T snv 1
rs2652106
VCAN
1.000 0.040 5 83498217 intron variant G/T snv 0.39 1
rs2479409
PCSK9
1.000 0.040 1 55038977 upstream gene variant G/A snv 0.66 4
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs2306691
LRP1-AS ; LRP1
1.000 0.040 12 57145019 missense variant A/G snv 2.0E-05 2.1E-05 1
rs2276109
MMP12
0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 18
rs2252070
MMP13
0.752 0.320 11 102955810 upstream gene variant C/T snv 0.68 13
rs2234681
MMP9
1.000 0.040 20 46008773 upstream gene variant ACACACACACACACACACACACAC/-;AC;ACAC;ACACAC;ACACACAC;ACACACACAC;ACACACACACAC;ACACACACACACAC;ACACACACACACACAC;ACACACACACACACACAC;ACACACACACACACACACAC;ACACACACACACACACACACAC;ACACACACACACACACACACACACAC;ACACACACACACACACACACACACACAC;ACACACACACACACACACACACACACACAC;ACACACACACACACACACACACACACACACAC;ACACACACACACACACACACACACACACACACAC delins 2
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs2070863
SERPINF2
1.000 0.040 17 1745208 missense variant C/G;T snv 0.24 1