"Institute of Human Genetics, FAU Erlangen, Friedrich-Alexander-Univer - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 599514	NM_001142966.3(GREB1L):c.111T>G (p.Phe37Leu)	GREB1L, LOC101927521 (F37L)	Single nucleotide variant (missense variant)	Short stature	GLikely pathogenic
Select item 599513	NM_001142966.3(GREB1L):c.988C>T (p.Arg330Trp)	GREB1L, LOC101927521 (R330W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance