ADGRL1[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2649419	NM_014921.5(ADGRL1):c.197C>T (p.Thr66Met)	ADGRL1 (T66M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3236589	NM_014921.5(ADGRL1):c.80G>A (p.Arg27Gln)	ADGRL1 (R27Q)	Single nucleotide variant (missense variant)	Developmental delay, behavioral abnormalities, and neuropsychiatric disorders	GUncertain significance
Select item 3087394	NM_014921.5(ADGRL1):c.79C>T (p.Arg27Trp)	ADGRL1 (R27W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1700603	NM_014921.5(ADGRL1):c.26G>A (p.Trp9Ter)	ADGRL1 (W9*)	Single nucleotide variant (nonsense)	Autistic behavior +1 more	GLikely pathogenic
Select item 2472996	NM_014921.5(ADGRL1):c.22C>G (p.Leu8Val)	ADGRL1 (L8V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2215900	NM_014921.5(ADGRL1):c.16G>A (p.Ala6Thr)	ADGRL1 (A6T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3234704	NM_014921.5(ADGRL1):c.13G>A (p.Ala5Thr)	ADGRL1 (A5T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3087397	NM_014921.5(ADGRL1):c.7C>T (p.Arg3Cys)	ADGRL1 (R3C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

ClinVar