List of variants in gene RET reported as uncertain significance by MGZ Medical Genetics Center

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_020975.6(RET):c.1942G>A (p.Val648Ile)	rs77711105	0.00005
NM_020975.6(RET):c.158T>C (p.Val53Ala)	rs2132659420
NM_020975.6(RET):c.1897_1899del (p.Leu633del)	rs2538493885

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