Related gene-specific medical variations for Gene (Select 23122) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3042518	NM_001365631.1(CLASP2):c.6G>A (p.Glu2=)	CLASP2, LOC129936446	Single nucleotide variant (synonymous variant +1 more)	CLASP2-related disorder	GLikely benign
Select item 3038051	NM_001365631.1(CLASP2):c.-20GCGG[4]	CLASP2, LOC129936446	Microsatellite (5 prime UTR variant)	CLASP2-related disorder	GLikely benign
Select item 2302377	NM_001365631.1(CLASP2):c.14G>T (p.Ser5Ile)	CLASP2, LOC129936446 (S5I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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