"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "LOC1299 - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2826204	NM_032119.4(ADGRV1):c.13C>T (p.Leu5=)	ADGRV1, LOC129994205	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2995076	NM_032119.4(ADGRV1):c.18G>T (p.Gly6=)	ADGRV1, LOC129994205	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 179382	NM_032119.4(ADGRV1):c.21A>C (p.Pro7=)	ADGRV1, LOC129994205	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2135612	NM_032119.4(ADGRV1):c.22+3A>C	ADGRV1, LOC129994205	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1469188	NM_032119.4(ADGRV1):c.22+6C>T	ADGRV1, LOC129994205	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2790506	NM_032119.4(ADGRV1):c.22+8A>G	ADGRV1, LOC129994205	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 193464	NM_032119.4(ADGRV1):c.22+9T>C	ADGRV1, LOC129994205	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 1923757	NM_032119.4(ADGRV1):c.22+12C>A	ADGRV1, LOC129994205	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2120924	NM_032119.4(ADGRV1):c.22+17G>T	ADGRV1, LOC129994205	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1139900	NM_032119.4(ADGRV1):c.22+17G>A	ADGRV1, LOC129994205	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2823785	NM_032119.4(ADGRV1):c.22+19G>C	ADGRV1, LOC129994205	Single nucleotide variant (intron variant)	not provided	GLikely benign