Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs20455
KIF6 ; LOC107986594
0.763 0.160 6 39357302 missense variant A/G snv 0.41 0.49 12
rs5065
NPPA ; CLCN6 ; NPPA-AS1
0.763 0.240 1 11846011 stop lost A/G snv 0.14 0.21 12
rs147377392
THBD
0.763 0.120 20 23048144 missense variant A/G snv 1.0E-04 2.8E-04 11
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 11
rs2228262
FSIP1 ; THBS1
0.763 0.200 15 39589977 missense variant A/G snv 7.9E-02 8.0E-02 10
rs41507953
EPHX2
0.790 0.280 8 27500988 missense variant A/G snv 8.7E-02 0.13 10
rs6859
NECTIN2
0.827 0.120 19 44878777 3 prime UTR variant A/G snv 0.58 10
rs6903956
ADTRP
0.763 0.160 6 11774350 intron variant A/G snv 0.65 10
rs2001844 0.882 0.040 8 125466503 upstream gene variant A/G snv 0.43 9
rs2576178
RNLS ; LIPJ
0.790 0.160 10 88583641 5 prime UTR variant A/G snv 0.29 9
rs10903323
MSRA
0.807 0.160 8 10292057 intron variant A/G snv 0.15 8
rs1467568
SIRT1
0.776 0.320 10 67915401 intron variant A/G snv 0.46 8
rs2288904
SLC44A2
0.807 0.240 19 10631494 missense variant A/G snv 0.80 0.83 8
rs10118757
MTAP
0.827 0.120 9 21853340 intron variant A/G snv 0.26 7
rs7944926
NADSYN1
0.807 0.200 11 71454579 intron variant A/G snv 0.54 7
rs12050217
BDKRB1
0.827 0.160 14 96262416 intron variant A/G snv 0.21 6
rs7136716 0.851 0.080 12 7538538 regulatory region variant A/G snv 0.22 6
rs7195830
CYBA
0.851 0.080 16 88643304 3 prime UTR variant A/G snv 0.62 0.69 6
rs139401390 0.851 0.120 10 88643382 regulatory region variant A/G snv 1.0E-02 5
rs372359132
MTRR
0.827 0.160 5 7878203 missense variant A/G snv 4.0E-06 2.1E-05 5
rs3828599
GPX3 ; LOC105378228
0.882 0.040 5 151022235 intron variant A/G snv 0.67 5
rs116092985
PKD1
0.882 0.040 16 2110972 missense variant A/G snv 6.5E-02 7.8E-02 4
rs2015086
CCL18
0.882 0.040 17 36064257 upstream gene variant A/G snv 0.22 4
rs4888378
CFDP1
0.851 0.040 16 75298143 intron variant A/G snv 0.52 4
rs12344245
FAM189A2
0.882 0.040 9 69340801 intron variant A/G snv 0.12 3