Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35440884 1.000 0.080 9 105051392 intron variant G/A snv 0.11 1
rs3847711 1.000 0.080 12 58440252 intergenic variant A/G snv 0.21 1
rs55864010 1.000 0.080 2 67474157 intergenic variant G/A snv 6.7E-02 1
rs61677309 1.000 0.080 11 118297371 intergenic variant A/T snv 0.32 1
rs66488313 1.000 0.080 6 26631340 downstream gene variant G/T snv 4.8E-02 1
rs6920364 1.000 0.080 6 166962978 intergenic variant G/A;C snv 1
rs77045810 1.000 0.080 1 168535779 downstream gene variant A/C snv 0.10 1
rs78154696 1.000 0.080 5 1000041 upstream gene variant G/A;T snv 1
rs78853063 1.000 0.080 11 57482553 downstream gene variant C/T snv 4.9E-02 1
rs79149102 1.000 0.080 15 74763478 regulatory region variant C/A;T snv 1
rs79368540 1.000 0.080 2 44962598 intron variant C/T snv 8.9E-02 1
rs79398649 1.000 0.080 5 1004587 upstream gene variant G/T snv 6.7E-02 1
rs78062588
ADAR
1.000 0.080 1 154593749 intron variant T/C snv 5.1E-02 1
rs3944100
AHR ; LOC105375170
1.000 0.080 7 17014722 intron variant T/C snv 0.30 1
rs3734542
BTN2A1
1.000 0.080 6 26468098 missense variant G/A;C snv 5.8E-02 6.4E-02 1
rs10436951
CEP170
1.000 0.080 1 243199378 intron variant A/G snv 7.1E-02 1
rs148791337
CROT
1.000 0.080 7 87356828 intron variant C/T snv 1.7E-02 1
rs60280813
CRTAC1
1.000 0.080 10 97913426 intron variant T/C snv 7.5E-02 1
rs12439944
CSK
1.000 0.080 15 74783309 intron variant G/A;T snv 1
rs2071460
CSNK2A3 ; GALNT18
1.000 0.080 11 11352722 missense variant A/G snv 0.48 0.41 1
rs501942
CYP21A2 ; SLC44A4
1.000 0.080 6 31872700 intron variant C/T snv 7.5E-02 1
rs116551911
DDR1
1.000 0.080 6 30896502 intron variant C/T snv 1
rs1057520037
EGFR
1.000 0.080 7 55174782 missense variant G/C snv 1
rs372594677
EPHA3
1.000 0.080 3 89472571 missense variant C/A;T snv 8.0E-06; 1.2E-05 1
rs2741348
EPHX2 ; GULOP
1.000 0.080 8 27563265 intron variant T/G snv 0.50 1