"Laboratory for Molecular Medicine, Mass General Brigham Personalized - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 256828	NM_000901.5(NR3C2):c.1497T>C (p.Asp499=)	NR3C2	Single nucleotide variant (synonymous variant +1 more)	not specified +2 more	GBenign
Select item 256832	NM_000901.5(NR3C2):c.538G>A (p.Val180Ile)	NR3C2 (V180I)	Single nucleotide variant (missense variant +1 more)	not specified +2 more	GBenign
Select item 256827	NM_000901.5(NR3C2):c.-2C>G	NR3C2	Single nucleotide variant (5 prime UTR variant +1 more)	not specified +2 more	GBenign

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