Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs769985775
DMD
0.851 0.160 X 32448630 synonymous variant T/C snv 5.7E-06 9.5E-06 6
rs17883901
GCLC
0.851 0.240 6 53545239 intron variant G/A;T snv 6.2E-02 6
rs2736654
GLO1
0.882 0.120 6 38682852 missense variant T/A;G snv 4
rs7533564
MGC27382 ; PTGFR
0.925 0.120 1 78360228 intron variant C/T snv 0.92 4
rs16995309
PTPN1
0.882 0.280 20 50581336 missense variant C/T snv 4.8E-03 5.0E-03 4
rs2518344
GRIK2
6 101327270 intron variant A/G snv 0.62 1
rs10499298
LOC101928923 ; LOC105378072
6 155812936 intergenic variant C/T snv 0.12 1
rs10499299
LOC105378072 ; LOC101928923
6 155812754 intergenic variant A/G snv 0.14 1
rs17827966
LOC105378072 ; LOC101928923
6 155817575 regulatory region variant T/C snv 0.12 1
rs713050
MRPL14
6 44124392 intron variant T/G snv 0.14 1