List of variants in gene SHOC2 reported as uncertain significance for Noonan syndrome

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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_007373.4(SHOC2):c.74A>G (p.Glu25Gly)	rs730881019	0.00008
NM_007373.4(SHOC2):c.1231A>G (p.Thr411Ala)	rs730881021
NM_007373.4(SHOC2):c.1741A>G (p.Met581Val)	rs1470655019
NM_007373.4(SHOC2):c.187G>A (p.Gly63Arg)
NM_007373.4(SHOC2):c.307A>G (p.Met103Val)

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