C1855733[trait identifier] AND "SIB Swiss Institute of Bioinformatics" - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1188814	NM_001982.4(ERBB3):c.2359A>C (p.Thr787Pro)	ERBB3 (T787P)	Single nucleotide variant (missense variant)	Visceral neuropathy, familial, 1, autosomal recessive	GLikely pathogenic
Select item 1188815	NM_001982.4(ERBB3):c.2695G>A (p.Val899Met)	ERBB3 (V899M)	Single nucleotide variant (missense variant)	Visceral neuropathy, familial, 1, autosomal recessive	GLikely pathogenic