List of variants in gene RET studied for Congenital central hypoventilation; Hirschsprung disease, susceptibility to, 1; Multiple endocrine neoplasia type 2B; Pheochromocytoma; Familial medullary thyroid carcinoma; Multiple endocrine neoplasia type 2A

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.2611G>A (p.Val871Ile)	rs145170911	0.00008
NM_020975.6(RET):c.2527G>A (p.Glu843Lys)	rs755837568	0.00006
NM_020975.6(RET):c.2371T>A (p.Tyr791Asn)	rs377767417	0.00004
NM_020975.6(RET):c.2225C>T (p.Thr742Met)	rs773256580	0.00003
NM_020975.6(RET):c.1151C>G (p.Pro384Arg)	rs771679592	0.00001
NM_020975.6(RET):c.1448A>G (p.Tyr483Cys)	rs752322996	0.00001
NM_020975.6(RET):c.2945G>A (p.Arg982His)	rs368550200	0.00001
NM_020975.6(RET):c.433G>A (p.Val145Ile)	rs1311922451	0.00001
NM_020975.6(RET):c.1852T>G (p.Cys618Gly)	rs76262710
NM_020975.6(RET):c.1947G>A (p.Ser649=)	rs377767412
NM_020975.6(RET):c.2454G>A (p.Glu818=)	rs794727131

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