List of variants in gene SHOC2 reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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_007373.4(SHOC2):c.-179T>A	rs143180451	0.00080
NM_007373.4(SHOC2):c.10A>C (p.Ser4Arg)	rs397517231	0.00004
NM_007373.4(SHOC2):c.-125C>T	rs188765124	0.00002
NM_007373.4(SHOC2):c.171C>T (p.Ser57=)	rs1554857645	0.00001
NM_007373.4(SHOC2):c.-66A>G	rs397517230

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