List of variants in gene SOS2 reported as likely benign by Service de Génétique Moléculaire,Hôpital Robert Debré

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: 7

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HGVS	dbSNP
NM_006939.4(SOS2):c.1339C>A (p.Pro447Thr)
NM_006939.4(SOS2):c.2261G>A (p.Ser754Asn)	rs181275468
NM_006939.4(SOS2):c.2317G>C (p.Asp773His)	rs114711076
NM_006939.4(SOS2):c.3088A>G (p.Thr1030Ala)	rs550680554
NM_006939.4(SOS2):c.549G>C (p.Leu183Phe)	rs137961578
NM_006939.4(SOS2):c.584G>C (p.Gly195Ala)
NM_006939.4(SOS2):c.709C>A (p.Pro237Thr)

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