List of variants reported as likely pathogenic for Laron syndrome

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000163.5(GHR):c.508G>C (p.Asp170His)	rs121909366	0.00001
NC_000005.10:g.(42700003_42711206)_(42719424_?)del
NM_000163.5(GHR):c.344A>C (p.Asn115Thr)	rs1579626395
NM_000163.5(GHR):c.618+792A>G	rs1011727375
NM_000163.5(GHR):c.70+5G>A	rs2112477601

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