List of variants in gene PHOX2B reported as likely benign 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.450C>G (p.Arg150=)	rs17881486	0.00412
NM_003924.4(PHOX2B):c.639C>G (p.Gly213=)	rs17879258	0.00039
NM_003924.4(PHOX2B):c.486C>T (p.Ala162=)	rs547677836

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