"PreventionGenetics, part of Exact Sciences"[submitter] AND "HCRTR2"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3042775	NM_001384272.1(HCRTR2):c.28C>T (p.Pro10Ser)	HCRTR2 (P10S)	Single nucleotide variant (missense variant)	HCRTR2-related disorder	GLikely benign
Select item 3043269	NM_001384272.1(HCRTR2):c.30C>T (p.Pro10=)	HCRTR2	Single nucleotide variant (synonymous variant)	HCRTR2-related disorder	GLikely benign
Select item 3044525	NM_001384272.1(HCRTR2):c.213G>A (p.Gly71=)	HCRTR2	Single nucleotide variant (synonymous variant)	HCRTR2-related disorder	GLikely benign
Select item 3037159	NM_001384272.1(HCRTR2):c.444C>T (p.Ile148=)	HCRTR2	Single nucleotide variant (synonymous variant)	HCRTR2-related disorder	GBenign
Select item 3042350	NM_001384272.1(HCRTR2):c.577T>A (p.Cys193Ser)	HCRTR2 (C193S)	Single nucleotide variant (missense variant)	HCRTR2-related disorder	GLikely benign
Select item 768101	NM_001384272.1(HCRTR2):c.846G>A (p.Thr282=)	HCRTR2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3059587	NM_001384272.1(HCRTR2):c.922A>G (p.Ile308Val)	HCRTR2 (I308V)	Single nucleotide variant (missense variant)	HCRTR2-related disorder	GBenign
Select item 714952	NM_001384272.1(HCRTR2):c.1292C>A (p.Thr431Lys)	HCRTR2 (T431K)	Single nucleotide variant (missense variant)	HCRTR2-related disorder +1 more	GLikely benign

ClinVar