"Illumina Laboratory Services, Illumina"[submitter] AND "PHOX2B-AS1"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 901843	NM_003924.4(PHOX2B):c.235G>A (p.Ala79Thr)	PHOX2B, PHOX2B-AS1 (A79T)	Single nucleotide variant (missense variant)	Neuroblastoma, susceptibility to, 2 +1 more	GUncertain significance
Select item 239587	NM_003924.4(PHOX2B):c.234C>T (p.Tyr78=)	PHOX2B-AS1, PHOX2B	Single nucleotide variant (synonymous variant)	not provided +5 more	GBenign/Likely benign
Select item 902754	NM_003924.4(PHOX2B):c.-105G>A	PHOX2B, PHOX2B-AS1	Single nucleotide variant (5 prime UTR variant)	Neuroblastoma, susceptibility to, 2 +1 more	GUncertain significance
Select item 902755	NM_003924.3(PHOX2B):c.-159C>T	PHOX2B-AS1, PHOX2B	Single nucleotide variant	Congenital central hypoventilation +1 more	GUncertain significance
Select item 348811	NM_003924.3(PHOX2B):c.-195G>A	PHOX2B, PHOX2B-AS1	Single nucleotide variant	Neuroblastoma, susceptibility to, 2 +1 more	GUncertain significance
Select item 348812	NM_003924.3(PHOX2B):c.-210C>A	PHOX2B, PHOX2B-AS1	Single nucleotide variant	Congenital central hypoventilation +1 more	GUncertain significance
Select item 348813	NM_003924.3(PHOX2B):c.-265G>A	PHOX2B, PHOX2B-AS1	Single nucleotide variant	Neuroblastoma, susceptibility to, 2 +1 more	GUncertain significance

ClinVar