Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11225395
MMP8
0.776 0.360 11 102725749 intron variant A/C;G snv 11
rs10033900
CFI
0.807 0.040 4 109737911 intron variant T/C snv 0.54 7
rs12423791
IGF1
0.925 0.040 12 102465050 intron variant G/C snv 2.8E-02 5
rs131451
MMP11 ; LOC107985577
0.882 0.120 22 23771357 intron variant C/T snv 0.82 4
rs13382811
ZEB2
0.882 0.040 2 144466053 intron variant C/T snv 0.21 4
rs5742632
LINC02456 ; IGF1
0.851 0.120 12 102462696 intron variant A/G snv 0.26 4
rs7839488
SNTB1
0.882 0.040 8 120550178 intron variant G/A snv 0.47 4
rs8027411
ANKRD34C-AS1
0.882 0.040 15 79168687 intron variant G/T snv 0.52 4
rs9330813
WNT7B
1.000 0.040 22 45968281 intron variant G/A;C snv 4
rs10453441
WNT7B
1.000 0.040 22 45967859 intron variant A/G snv 0.40 3
rs10500355
RBFOX1
0.925 0.040 16 7409346 intron variant T/A snv 0.29 3
rs10824518
KCNMA1
0.882 0.040 10 77303784 intron variant T/A;C snv 3
rs12193446
LAMA2 ; LOC102723409
0.925 0.040 6 129498893 intron variant A/G snv 6.4E-02 3
rs12716080
CTNND2
0.882 0.040 5 11166836 intron variant G/T snv 0.39 3
rs1867315
RASGRF1 ; LOC100129540
0.882 0.120 15 78977393 intron variant C/G;T snv 3
rs577948
MIR100HG
0.882 0.040 11 122159482 intron variant A/G snv 0.33 3
rs6469937
SNTB1
0.882 0.040 8 120598198 intron variant G/A snv 0.48 3
rs6885224
CTNND2
0.882 0.040 5 11169833 intron variant C/A;T snv 3
rs7744813
KCNQ5
0.925 0.040 6 72933566 intron variant C/A snv 0.66 3
rs9318086
MIPEP
0.882 0.040 13 23858328 intron variant A/G snv 0.55 3
rs1635529
COL2A1
0.925 0.040 12 48001319 intron variant T/G snv 0.78 2
rs2973644
FGF10
0.925 0.040 5 44384081 intron variant C/A;T snv 2
rs3026393
ELP4 ; PAX6
0.925 0.040 11 31790667 intron variant A/C;G;T snv 0.48; 8.0E-06; 7.6E-05 2
rs339501
FGF10
0.925 0.040 5 44365531 intron variant C/T snv 0.94 2
rs498186
WTAPP1 ; MMP1
0.925 0.080 11 102798914 intron variant A/C snv 0.40 2