List of variants in gene RET reported as likely pathogenic by Laboratory of Molecular Epidemiology of Birth Defects, West China Second University Hospital, Sichuan University

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.2410G>A (p.Val804Met)	rs79658334	0.00022
NM_020975.6(RET):c.1189G>A (p.Val397Met)	rs183729115	0.00001
NM_020975.6(RET):c.3021G>C (p.Lys1007Asn)	rs786204098
NM_020975.6(RET):c.818C>A (p.Pro273His)	rs2132708181

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