List of variants in gene GREB1L reported as pathogenic by Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen

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_001142966.3(GREB1L):c.1975C>T (p.Gln659Ter)
NM_001142966.3(GREB1L):c.2614_2615del (p.Leu872fs)
NM_001142966.3(GREB1L):c.4992T>A (p.Tyr1664Ter)

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