List of variants in gene RET reported as benign by Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.2508C>T (p.Ser836=)	rs1800862	0.03791
NM_020975.6(RET):c.1264-5C>T	rs9282835	0.02749
NM_020975.6(RET):c.2944C>T (p.Arg982Cys)	rs17158558	0.01651
NM_020975.6(RET):c.375C>A (p.Val125=)	rs1800859	0.00877
NM_020975.6(RET):c.1465G>A (p.Asp489Asn)	rs9282834	0.00106
NM_020975.6(RET):c.833C>A (p.Thr278Asn)	rs35118262	0.00056

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