List of variants in gene RET reported as likely pathogenic by Fulgent Genetics, Fulgent Genetics

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.3185A>G (p.Tyr1062Cys)	rs587778659	0.00003
NM_020975.6(RET):c.1947G>A (p.Ser649=)	rs377767412
NM_020975.6(RET):c.1998G>C (p.Lys666Asn)	rs146646971
NM_020975.6(RET):c.2672C>T (p.Ser891Leu)
NM_020975.6(RET):c.2914A>G (p.Arg972Gly)	rs76534745

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