RS2145431062 RTEL1

Health Risk Chr 20:63690211
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Associated Conditions
Dyskeratosis congenita
autosomal recessive 5
Pulmonary fibrosis and/or bone marrow failure
Telomere-related
3
Combined oxidative phosphorylation defect type 24
Dyskeratosis congenita
autosomal recessive 5
Pulmonary fibrosis and/or bone marrow failure
Telomere-related
3
Combined oxidative phosphorylation defect type 24
Other Variants in RTEL1
rs201540674 rs370343781 rs398123017 rs398123018 rs587777037 rs398123048 rs398123050 rs398123051 rs373740199 rs398123052
Ask Dr. Hemsworth about this variant