ClinVar Miner

List of variants reported as uncertain significance for Acute myeloid leukemia; Dyskeratosis congenita, autosomal dominant 2; Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 1; Melanoma, cutaneous malignant, susceptibility to, 9

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_198253.3(TERT):c.1317GGA[2] (p.Glu441del)	rs377639087
NM_198253.3(TERT):c.2221G>A (p.Val741Met)	rs150819225
NM_198253.3(TERT):c.902G>A (p.Arg301His)	rs1268051204

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