List of variants in gene RET reported as benign by Mendelics

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: 13

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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.833C>A (p.Thr278Asn)	rs35118262	0.00056
NM_020975.6(RET):c.1946C>T (p.Ser649Leu)	rs148935214	0.00039
NM_020975.6(RET):c.1529C>T (p.Ala510Val)	rs201745826	0.00019
NM_020975.6(RET):c.3188-9C>T	rs551159582	0.00005
NM_020975.6(RET):c.1118C>T (p.Ala373Val)	rs546866208	0.00004
NM_020975.6(RET):c.539G>A (p.Arg180Gln)	rs370736139	0.00003
NM_020975.6(RET):c.1941C>T (p.Ile647=)	rs75225191	0.00002
NM_020975.6(RET):c.3332C>T (p.Thr1111Met)	rs1003057639	0.00001
NM_020975.6(RET):c.1468C>G (p.Gln490Glu)	rs1588871393
NM_020975.6(RET):c.2765C>A (p.Ser922Tyr)	rs377767432
NM_020975.6(RET):c.74-50G>T	rs766786245
NM_020975.6(RET):c.742G>A (p.Gly248Ser)	rs1837733775

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