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
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 15
rs4820268
TMPRSS6
0.851 0.160 22 37073551 missense variant G/A;C snv 0.53; 4.0E-06 14
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs198846
H1-6
6 26107235 downstream gene variant A/G;T snv 7
rs129128
H2BC4 ; H2AC6
6 26125114 intron variant C/T snv 0.91 7
rs130624 22 37042611 regulatory region variant G/T snv 0.47 6
rs228129
LOC112268295
22 37032558 upstream gene variant A/G snv 0.48 6
rs2413450
TMPRSS6
22 37074184 intron variant T/C snv 0.61 6
rs198833 6 26114280 downstream gene variant G/A snv 0.87 5
rs10495928
PRKCE
2 46126027 intron variant A/G snv 0.36 5
rs11089823 22 37113139 upstream gene variant T/C snv 0.28 4
rs11089824 22 37113146 upstream gene variant A/C;T snv 4
rs763668 22 37115036 intergenic variant C/G;T snv 4
rs16926246
HK1
10 69333636 intron variant C/T snv 0.12 4
rs5750373
MPST
22 37028990 non coding transcript exon variant G/A snv 0.49 4
rs5756520
TMPRSS6
22 37112467 upstream gene variant G/A snv 0.41 4
rs11914132 22 37113047 upstream gene variant C/T snv 0.27 3
rs228918
TMPRSS6
22 37110640 upstream gene variant T/C snv 0.40 3
rs228919
TMPRSS6
22 37110673 upstream gene variant G/T snv 0.40 3
rs228921
TMPRSS6
22 37110836 upstream gene variant A/G snv 0.41 3
rs6013509 20 52701812 downstream gene variant G/A;C snv 2