Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1186757238
PDE4D
1.000 0.040 5 59039089 5 prime UTR variant A/C snv 2
rs12315434
R3HDM2
1.000 0.040 12 57387153 intron variant A/C snv 0.16 2
rs2128739 0.925 0.080 11 103802549 intron variant A/C snv 0.68 2
rs2965169
BCL3
0.925 0.120 19 44747899 non coding transcript exon variant A/C snv 0.50 2
rs4932373
FES
1.000 0.040 15 90886057 intron variant A/C snv 0.25 2
rs498186
WTAPP1 ; MMP1
0.925 0.080 11 102798914 intron variant A/C snv 0.40 2
rs11057840
SCARB1
1.000 0.040 12 124831509 intron variant A/C snv 0.16 1
rs11913721
MAPK1
1.000 0.040 22 21855846 intron variant A/C snv 0.34 1
rs13118820
LOC105377505
1.000 0.040 4 155515365 intron variant A/C snv 0.63 1
rs145099029 1.000 0.040 6 160871806 downstream gene variant A/C snv 2.6E-03 1
rs1476098
BCAS3
1.000 0.040 17 61159652 intron variant A/C snv 0.66 1
rs1780050
NEXN
1.000 0.040 1 77934855 intron variant A/C snv 0.37 1
rs1807214 1.000 0.040 15 89022026 regulatory region variant A/C snv 0.29 1
rs2738447
LDLR
1.000 0.040 19 11116804 intron variant A/C snv 0.65 1
rs4613862
LINC02542
1.000 0.040 6 81902554 intron variant A/C snv 0.37 1
rs4621175
GALNT3
1.000 0.040 2 165792282 intron variant A/C snv 0.80 1
rs4644046 1.000 0.040 6 51520211 intergenic variant A/C snv 0.38 1
rs5029930
WAKMAR2 ; TNFAIP3
1.000 0.040 6 137869547 intron variant A/C snv 0.20 1
rs56170783
PLPP3
1.000 0.040 1 56550459 intron variant A/C snv 6.5E-02 1
rs6740322
THADA
1.000 0.040 2 43334790 intron variant A/C snv 0.20 1
rs7678555 1.000 0.040 4 119988346 intergenic variant A/C snv 0.23 1
rs9964304
LOC105372112
1.000 0.040 18 49703347 intergenic variant A/C snv 0.33 1
rs14259
PSMD9
0.724 0.360 12 121915890 missense variant A/C;G snv 4.0E-06; 0.32 19
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs879254642
LDLR
0.882 0.120 19 11105589 missense variant A/C;G snv 6