List of variants in gene RET reported as uncertain significance by OMIM

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.2372A>T (p.Tyr791Phe)	rs77724903	0.00178
NM_020975.6(RET):c.341G>A (p.Arg114His)	rs76397662	0.00039
NM_020975.6(RET):c.2332G>A (p.Val778Ile)	rs75686697	0.00003
NM_020975.6(RET):c.592C>A (p.Pro198Thr)	rs76736111

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