"PreventionGenetics, part of Exact Sciences"[submitter] AND "TMEM50B"[ - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 717050	NM_005534.4(IFNGR2):c.756C>T (p.Ser252=)	IFNGR2, TMEM50B	Single nucleotide variant (synonymous variant +1 more)	not provided +2 more	GLikely benign
Select item 474971	NM_005534.4(IFNGR2):c.978G>A (p.Pro326=)	IFNGR2, TMEM50B	Single nucleotide variant (synonymous variant)	IFNGR2-related disorder +2 more	GBenign/Likely benign