List of variants in gene RET reported as benign for Ovarian cancer

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.224C>T (p.Thr75Met)	rs142641173	0.00006
NM_020975.6(RET):c.406G>A (p.Glu136Lys)	rs79014735	0.00004
NM_020975.6(RET):c.1216A>G (p.Ser406Gly)	rs756532455	0.00002
NM_020975.6(RET):c.220G>A (p.Gly74Ser)	rs764938319	0.00002
NM_020975.6(RET):c.1052T>A (p.Val351Glu)	rs749449032	0.00001
NM_020975.6(RET):c.1618A>G (p.Arg540Gly)	rs543376293	0.00001
NM_020975.6(RET):c.1385C>T (p.Ser462Leu)	rs1313331250
NM_020975.6(RET):c.376T>C (p.Phe126Leu)	rs2132678531
NM_020975.6(RET):c.733G>A (p.Val245Met)	rs1837733068
NM_020975.6(RET):c.959C>T (p.Pro320Leu)	rs1837779952

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