RS786204108 TFR2

Health Risk Chr 7:100626866
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What This Variant Does
"CLNSIG=4
Associated Conditions
Hereditary hemochromatosis
Hemochromatosis type 3
Hereditary hemochromatosis
Hemochromatosis type 3
Other Variants in TFR2
rs80338880 rs80338877 rs80338879 rs41303501 rs80338889 rs80338882 rs80338883 rs80338884 rs80338885 rs80338888
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