List of variants in gene combination LOC110806263, TERT reported as uncertain significance for bone marrow disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_198253.3(TERT):c.159G>C (p.Gln53His)	rs1060503006	0.00006
NM_198253.3(TERT):c.150G>A (p.Leu50=)	rs886044153	0.00003
NM_198253.3(TERT):c.124G>C (p.Gly42Arg)	rs1751293669

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