List of variants in gene RET reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.166C>A (p.Leu56Met)	rs145633958	0.00310
NM_020975.6(RET):c.1336G>C (p.Gly446Arg)	rs115423919	0.00238
NM_020975.6(RET):c.833C>A (p.Thr278Asn)	rs35118262	0.00056
NM_020975.6(RET):c.2673G>A (p.Ser891=)	rs201620214	0.00027
NM_020975.6(RET):c.2547C>T (p.Gly849=)	rs770674650	0.00001

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