List of variants in gene SOS2 reported as 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_006939.4(SOS2):c.2232C>T (p.Asn744=)	rs2229869	0.59746
NM_006939.4(SOS2):c.816T>C (p.Ser272=)	rs35396088	0.02070
NM_006939.4(SOS2):c.591A>G (p.Leu197=)	rs113460230	0.00834
NM_006939.4(SOS2):c.3813G>A (p.Pro1271=)	rs2227276

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