Related gene-specific medical variations for Gene (Select 7869) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3029421	NM_001290060.2(SEMA3B):c.696G>A (p.Pro232=)	LOC129936787, SEMA3B	Single nucleotide variant (synonymous variant +2 more)	SEMA3B-related disorder	GLikely benign
Select item 2634858	NM_001290060.2(SEMA3B):c.689G>T (p.Trp230Leu)	LOC129936787, SEMA3B (W230L)	Single nucleotide variant (missense variant +2 more)	SEMA3B-related disorder	GUncertain significance