List of variants in gene RET reported as likely benign for Hirschsprung Disease, Dominant

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.*1742G>A	rs143369221	0.00349
NM_020975.6(RET):c.337+12G>A	rs200468424	0.00198
NM_020975.6(RET):c.1118C>T (p.Ala373Val)	rs546866208	0.00017
NM_020975.6(RET):c.*499dup	rs201945709

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