C1970712[trait identifier] AND "Institute of Human Genetics, Universit - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 13936	NM_020975.6(RET):c.2372A>T (p.Tyr791Phe)	RET (Y791F +17 more)	Single nucleotide variant (missense variant)	not specified +9 more	GBenign/Likely benign
Select item 217126	NM_004064.5(CDKN1B):c.-31AG[1]	CDKN1B	Microsatellite (5 prime UTR variant)	Multiple endocrine neoplasia +4 more	GConflicting classifications of pathogenicity
Select item 2576587	NM_004064.5(CDKN1B):c.18_23delinsT (p.Ser7fs)	CDKN1B (S7fs)	Indel (frameshift variant)	Multiple endocrine neoplasia type 4	GLikely pathogenic

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