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
rs863223904
ALAS2
0.827 0.200 X 55014829 missense variant C/T snv 6.1E-06 5
rs80356713
ABCB7
0.925 0.120 X 75070499 missense variant C/A;G snv 3
rs201062903
ALAS2
0.882 0.120 X 55013527 missense variant G/A snv 1.3E-03 1.2E-03 3
rs541845688
ABCB6
0.925 0.160 2 219210782 missense variant C/T snv 4.4E-05 7.0E-06 2
rs797044558
ABCB7
0.925 0.160 X 75053585 missense variant C/T snv 2
rs1557248142
ALAS2
0.925 0.080 X 55021182 missense variant G/T snv 2
rs892041887
ALAS2 ; APEX2
0.925 0.080 X 55009265 missense variant C/T snv 2
rs1460260991
ALAS1
1.000 0.040 3 52203996 synonymous variant A/G snv 4.1E-06 1
rs200361165
ALAS1
1.000 0.040 3 52212412 missense variant A/C;G snv 1.2E-05 1