Disease: Hemoglobin, CTCAE
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 38
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 17
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs2413450
TMPRSS6
22 37074184 intron variant T/C snv 0.61 6
rs10495928
PRKCE
2 46126027 intron variant A/G snv 0.36 5
rs16926246
HK1
10 69333636 intron variant C/T snv 0.12 4