List of variants in gene SHOC2 reported as benign for Noonan syndrome and Noonan-related syndrome

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_007373.4(SHOC2):c.457C>T (p.Leu153=)	rs34081996	0.01281
NM_007373.4(SHOC2):c.1423-7C>T	rs180671383	0.00563
NM_007373.4(SHOC2):c.*3T>C	rs143187497	0.00097
NM_007373.4(SHOC2):c.1161+9A>G	rs201795589	0.00008
NM_007373.4(SHOC2):c.1541-7del	rs371544139
NM_007373.4(SHOC2):c.973-5del	rs730881016

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