"PreventionGenetics, part of Exact Sciences"[submitter] AND "GRPR"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 721453	NM_005314.3(GRPR):c.17G>C (p.Cys6Ser)	GRPR (C6S)	Single nucleotide variant (missense variant)	GRPR-related disorder +1 more	GLikely benign
Select item 3051058	NM_005314.3(GRPR):c.110C>T (p.Pro37Leu)	GRPR (P37L)	Single nucleotide variant (missense variant)	GRPR-related disorder	GLikely benign
Select item 790473	NM_005314.3(GRPR):c.396G>A (p.Thr132=)	GRPR	Single nucleotide variant (synonymous variant)	GRPR-related disorder +1 more	GBenign
Select item 753760	NM_005314.3(GRPR):c.504C>T (p.Ser168=)	GRPR	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3053094	NM_005314.3(GRPR):c.784C>G (p.Leu262Val)	GRPR (L262V)	Single nucleotide variant (missense variant)	GRPR-related disorder	GLikely benign
Select item 788755	NM_005314.3(GRPR):c.1011G>C (p.Leu337=)	GRPR	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 748394	NM_005314.3(GRPR):c.1086G>A (p.Lys362=)	GRPR	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign

ClinVar