Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4746
GLO1
0.708 0.400 6 38682852 missense variant T/A;G snv 0.36 21
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs696217
GHRL ; GHRLOS
0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs713041
GPX4
0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 16
rs713050
MRPL14
6 44124392 intron variant T/G snv 0.14 1
rs7533564
MGC27382 ; PTGFR
0.925 0.120 1 78360228 intron variant C/T snv 0.92 4
rs769985775
DMD
0.851 0.160 X 32448630 synonymous variant T/C snv 5.7E-06 9.5E-06 6
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98