"Ambry Genetics"[submitter] AND "LOC129936788"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1301689	NM_006764.5(IFRD2):c.47G>A (p.Arg16His)	IFRD2, LOC129936788 (R16H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108339	NM_006764.5(IFRD2):c.38G>A (p.Gly13Asp)	IFRD2, LOC129936788 (G13D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244021	NM_006764.5(IFRD2):c.5C>G (p.Pro2Arg)	IFRD2, LOC129936788 (P2R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461608	NM_006764.5(IFRD2):c.-11C>G	IFRD2, LOC129936788	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 2368607	NM_006764.5(IFRD2):c.-26C>T	IFRD2, LOC129936788	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 2323155	NM_006764.5(IFRD2):c.-39G>A	IFRD2, LOC129936788	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance

ClinVar