Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4784677
BBS2
1.000 0.120 16 56514589 missense variant C/T snv 0.99 1.00 1
rs820878
HEXB
1.000 0.120 5 74685445 missense variant T/C snv 0.97 0.97 1
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 4
rs4302331
GLB1
1.000 0.120 3 33014229 missense variant A/G snv 0.98 0.93 1
rs2241880
SCARNA5 ; ATG16L1
0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 1
rs2071460
CSNK2A3 ; GALNT18
1.000 0.080 11 11352722 missense variant A/G snv 0.48 0.41 1
rs2236225
MTHFD1
0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 1
rs12150220
NLRP1
0.724 0.360 17 5582047 missense variant A/T snv 0.37 0.33 1
rs61749665
GUCY2D
1.000 0.040 17 8003201 missense variant G/T snv 0.42 0.30 1
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 1
rs1801265
DPYD
0.763 0.280 1 97883329 missense variant A/G snv 0.28 1
rs351855
FGFR4
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 1
rs9925969
PKD1
1.000 0.120 16 2102386 missense variant A/G snv 0.16 0.25 1
rs10151259
RPGRIP1
1.000 0.080 14 21321881 missense variant G/T snv 0.20 0.22 1
rs2549677
PKD1
1.000 0.120 16 2112360 missense variant A/G snv 7.2E-02 0.21 1
rs9936785
PKD1
1.000 0.120 16 2105425 missense variant T/C snv 4.4E-02 0.19 1
rs1803274
BCHE
0.763 0.360 3 165773492 missense variant C/T snv 0.18 0.18 1
rs6811423
DOK7
1.000 0.080 4 3492873 missense variant A/G snv 0.23 0.18 1
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 2
rs3829868
CRNN ; FLG-AS1
0.925 0.080 1 152409644 missense variant C/T snv 0.21 0.15 1
rs1566734
PTPRJ
0.807 0.120 11 48123823 missense variant A/C snv 0.17 0.15 1
rs36094464
DSPP
1.000 0.080 4 87612388 missense variant A/T snv 8.5E-02 0.14 1
rs2275272
ALDH18A1
1.000 0.280 10 95628405 missense variant G/A snv 0.11 0.10 1
rs33980500
TRAF3IP2-AS1 ; TRAF3IP2
0.742 0.200 6 111592059 missense variant C/T snv 8.6E-02 9.7E-02 1
rs7014851
HR
1.000 0.080 8 22119197 missense variant T/C snv 3.1E-02 8.6E-02 1