List of variants reported as pathogenic for isolated congenital growth hormone deficiency by Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_003401.5(XRCC4):c.127T>C (p.Trp43Arg)	rs587779351	0.00002
NM_000059.4(BRCA2):c.9152del (p.Pro3051fs)	rs587779349
NM_014171.6(CRIPT):c.133_134insGG (p.Ala45fs)	rs587779356
NM_014171.6(CRIPT):c.141del (p.Phe47fs)	rs587779348

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