"MTNR1B-related disorder"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3058891	NM_005959.5(MTNR1B):c.71G>A (p.Gly24Glu)	MTNR1B (G24E)	Single nucleotide variant (missense variant)	MTNR1B-related disorder	GBenign
Select item 3056447	NM_005959.5(MTNR1B):c.336C>T (p.His112=)	MTNR1B	Single nucleotide variant (synonymous variant)	MTNR1B-related disorder	GLikely benign
Select item 719914	NM_005959.5(MTNR1B):c.504C>T (p.Thr168=)	MTNR1B	Single nucleotide variant (synonymous variant)	MTNR1B-related disorder +1 more	GLikely benign
Select item 3051832	NM_005959.5(MTNR1B):c.593C>A (p.Thr198Asn)	MTNR1B (T198N)	Single nucleotide variant (missense variant)	MTNR1B-related disorder	GLikely benign
Select item 3060517	NM_005959.5(MTNR1B):c.728A>G (p.Lys243Arg)	MTNR1B (K243R)	Single nucleotide variant (missense variant)	MTNR1B-related disorder	GBenign
Select item 3043615	NM_005959.5(MTNR1B):c.816C>T (p.Leu272=)	MTNR1B	Single nucleotide variant (synonymous variant)	MTNR1B-related disorder	GLikely benign
Select item 3053421	NM_005959.5(MTNR1B):c.974C>T (p.Ala325Val)	MTNR1B (A325V)	Single nucleotide variant (missense variant)	MTNR1B-related disorder	GBenign

ClinVar