RS373740199 RTEL1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Dyskeratosis congenita
autosomal dominant 4
autosomal recessive 5
Pulmonary fibrosis and/or bone marrow failure
Telomere-related
3
Pulmonary fibrosis
RTEL1-related disorder
Adams-Oliver syndrome 3
Dyskeratosis congenita
autosomal dominant 4
autosomal recessive 5
Pulmonary fibrosis and/or bone marrow failure
Telomere-related
3
Other Variants in RTEL1