"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "GOSR2"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 205628	NM_004287.5(GOSR2):c.111C>T (p.Ile37=)	LRRC37A2, GOSR2 +1 more	Single nucleotide variant (synonymous variant +1 more)	Inborn genetic diseases +4 more	GBenign/Likely benign
Select item 30406	NM_004287.5(GOSR2):c.430G>T (p.Gly144Trp)	GOSR2, LRRC37A2 (G144W +2 more)	Single nucleotide variant (missense variant +2 more)	not provided +2 more	GPathogenic
Select item 205631	NM_004287.5(GOSR2):c.509A>G (p.Asn170Ser)	GOSR2, LRRC37A2 (N170S +5 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +3 more	GUncertain significance
Select item 585946	NM_004287.5(GOSR2):c.*1795G>C	GOSR2, LRRC37A2 (G195A +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not provided	GUncertain significance
Select item 383352	NM_004287.5(GOSR2):c.*1823C>T	LRRC37A2, GOSR2	Single nucleotide variant (3 prime UTR variant +2 more)	not provided +2 more	GBenign/Likely benign
Select item 2582959	NM_001321133.2(GOSR2):c.750A>G (p.Leu250=)	GOSR2, LRRC37A2	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign

ClinVar