ClinVar Miner

List of variants reported as likely benign for Hypochondroplasia

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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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