RS398123018 RTEL1

Health Risk Chr 20:63693160
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What This Variant Does
"CLNSIG=5
Associated Conditions
Dyskeratosis congenita
autosomal recessive 5
Pulmonary fibrosis and/or bone marrow failure
Telomere-related
3
RTEL1-related disorder
Dyskeratosis congenita
autosomal recessive 5
Pulmonary fibrosis and/or bone marrow failure
Telomere-related
3
Inborn genetic diseases
Dyskeratosis congenita
autosomal recessive 5
Pulmonary fibrosis and/or bone marrow failure
Other Variants in RTEL1
rs201540674 rs370343781 rs398123017 rs587777037 rs398123048 rs398123050 rs398123051 rs373740199 rs398123052 rs863223336
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