Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17576
MMP9
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 110
rs2375801
MTNR1A
4 186550471 intron variant T/C snv 0.34 1
rs2660852 12 96051770 intergenic variant C/A snv 0.34 3
rs353630
CD44
1.000 0.080 11 35166644 intron variant G/A snv 0.33 1
rs6475526 1.000 0.080 9 21242162 upstream gene variant C/T snv 0.33 2
rs10491121
LOC101927369 ; CCL4
0.882 0.120 17 36102943 upstream gene variant G/A snv 0.32 5
rs1536309
MIR146B
0.851 0.160 10 102435445 upstream gene variant A/G snv 0.32 7
rs7553007 0.827 0.120 1 159728759 intergenic variant G/A snv 0.31 6
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 45
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 103
rs746429
SIPA1
0.882 0.120 11 65649963 synonymous variant G/A snv 0.31 0.30 8
rs16940
BRCA1
0.882 0.080 17 43093220 synonymous variant A/G snv 0.35 0.29 5
rs3790843
NR5A2
0.827 0.160 1 200041696 intron variant C/T snv 0.29 7
rs4647958
SNAI1
0.851 0.080 20 49984094 missense variant T/C snv 0.18 0.29 5
rs486907
RNASEL
0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 31
rs3804639
CD47
3 108071988 intron variant G/T snv 0.28 1
rs3206652
CD47
3 108046402 3 prime UTR variant T/C snv 0.27 1
rs684559
CHI3L2
1 111215824 intron variant G/A snv 0.27 1
rs3774937
NFKB1
0.776 0.280 4 102513096 intron variant T/C snv 0.26 4
rs351855
FGFR4
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 55
rs3212227
IL12B
0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs7646409
PIK3CA
0.882 0.040 3 179182405 intron variant T/C snv 0.26 4
rs1472189
DKK3
11 11962338 3 prime UTR variant C/T snv 0.25 1
rs2055979
IL21-AS1 ; IL21
0.827 0.320 4 122619586 intron variant C/A snv 0.23 6