"PreventionGenetics, part of Exact Sciences"[submitter] AND "NGF-AS1"[ - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3040020	NM_002506.3(NGF):c.681G>C (p.Thr227=)	NGF, NGF-AS1	Single nucleotide variant (synonymous variant)	NGF-related disorder	GLikely benign
Select item 291991	NM_002506.3(NGF):c.239G>A (p.Arg80Gln)	NGF, NGF-AS1 (R80Q)	Single nucleotide variant (missense variant)	NGF-related disorder +2 more	GBenign/Likely benign
Select item 526751	NM_002506.3(NGF):c.174G>A (p.Ala58=)	NGF-AS1, NGF	Single nucleotide variant (synonymous variant)	Congenital sensory neuropathy with selective loss of small myelinated fibers +1 more	GConflicting classifications of pathogenicity
Select item 456627	NM_002506.3(NGF):c.173C>T (p.Ala58Val)	NGF, NGF-AS1 (A58V)	Single nucleotide variant (missense variant)	Congenital sensory neuropathy with selective loss of small myelinated fibers +2 more	GBenign/Likely benign
Select item 384001	NM_002506.3(NGF):c.78C>T (p.Val26=)	NGF, NGF-AS1	Single nucleotide variant (synonymous variant)	NGF-related disorder +2 more	GBenign/Likely benign
Select item 291994	NM_002506.3(NGF):c.54G>A (p.Ala18=)	NGF, NGF-AS1	Single nucleotide variant (synonymous variant)	NGF-related disorder +2 more	GBenign

ClinVar