List of variants in gene PHOX2B reported as pathogenic for neuroblastoma, susceptibility to, 2

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_003924.4(PHOX2B):c.778_779insGGCGGCGGCGGCAGCGGCAGCGGCGGCAGC (p.Ala260delinsGlyArgArgArgGlnArgGlnArgArgGlnPro)
NM_003924.4(PHOX2B):c.866dup (p.Pro290fs)	rs1733868277
NM_003924.4(PHOX2B):c.945A>C (p.Ter315Cys)	rs1553897738

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