SLC11A2, solute carrier family 11 member 2, 4891

N. diseases: 99; N. variants: 13
Disease: ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 1 ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs121918365
rs121918365 		0.882 0.080 12 50992810 missense variant C/G snv 1.4E-05
CUI: C3806153
Disease: ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 1
ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 1 		0.700 1.000 3 2005 2006
dbSNP: rs121918366
rs121918366 		0.827 0.160 12 50992291 missense variant G/A;C snv
CUI: C3806153
Disease: ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 1
ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 1 		0.700 1.000 3 2005 2006
dbSNP: rs121918367
rs121918367 		0.827 0.080 12 50999214 missense variant C/A;T snv 6.0E-05
CUI: C3806153
Disease: ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 1
ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 1 		0.700 1.000 3 2005 2006