RS149566858 TERT

Health Risk Chr 5:1278750
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What This Variant Does
"CLNSIG=5
Associated Conditions
Dyskeratosis congenita
autosomal dominant 1
Interstitial lung disease 2
Idiopathic Pulmonary Fibrosis
autosomal dominant 2
TERT-related disorder
Melanoma
cutaneous malignant
susceptibility to
9
Pulmonary fibrosis and/or bone marrow failure
Telomere-related
1
Acute myeloid leukemia
Dyskeratosis congenita
Other Variants in TERT
rs121918661 rs34094720 rs121918662 rs121918665 rs121918666 rs199422300 rs199422309 rs199422294 rs199422301 rs199422304
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