List of variants in gene combination GH-LCR, GH1 reported as likely benign for isolated congenital growth hormone deficiency

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000515.5(GH1):c.116C>T (p.Ala39Val)	rs151263636	0.00985
NM_000515.4(GH1):c.-68A>G	rs6171
NM_000515.5(GH1):c.-63A>C	rs695
NM_000515.5(GH1):c.-63A>T	rs695
NM_000515.5(GH1):c.456+19G>T	rs61735351

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