ClinVar Miner

List of variants in gene RNPC3 reported as benign for isolated congenital growth hormone deficiency

Included ClinVar conditions (10):

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_017619.4(RNPC3):c.359+16A>G	rs6702220	0.68079
NM_017619.4(RNPC3):c.342C>T (p.Gly114=)	rs6697444	0.64524

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