RS587777037 RTEL1

Health Risk Chr 20:63695558
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Dyskeratosis congenita
autosomal recessive 5
Inborn genetic diseases
Pulmonary fibrosis and/or bone marrow failure
Telomere-related
3
Dyskeratosis congenita
autosomal recessive 5
Inborn genetic diseases
Pulmonary fibrosis and/or bone marrow failure
Telomere-related
3
Other Variants in RTEL1
rs201540674 rs370343781 rs398123017 rs398123018 rs398123048 rs398123050 rs398123051 rs373740199 rs398123052 rs863223336
Ask Dr. Hemsworth about this variant