List of variants in gene FGFR3 reported as likely benign for Hypochondroplasia

Minimum submission review status:		Collection method:
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: 3

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HGVS	dbSNP
NM_000142.4(FGFR3):c.514G>A (p.Val172Ile)	rs529408918
NM_000142.5(FGFR3):c.1150T>C (p.Phe384Leu)	rs17881656
NM_000142.5(FGFR3):c.1345C>T (p.Pro449Ser)	rs61735104

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