List of variants in gene RET reported as pathogenic for MEN2 phenotype: Unclassified

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.2410G>A (p.Val804Met)	rs79658334	0.00022
NM_020975.6(RET):c.2671T>G (p.Ser891Ala)	rs75234356	0.00001
NM_020975.6(RET):c.1832G>A (p.Cys611Tyr)	rs377767397
NM_020975.6(RET):c.1859G>C (p.Cys620Ser)	rs77503355
NM_020975.6(RET):c.1900T>G (p.Cys634Gly)	rs75076352
NM_020975.6(RET):c.1998G>C (p.Lys666Asn)	rs146646971
NM_020975.6(RET):c.2304G>T (p.Glu768Asp)	rs78014899
NM_020975.6(RET):c.2410G>C (p.Val804Leu)	rs79658334

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