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	gnomAD frequency
NM_006939.4(SOS2):c.549G>C (p.Leu183Phe)	rs137961578	0.00083
NM_006939.4(SOS2):c.2317G>C (p.Asp773His)	rs114711076	0.00040
NM_006939.4(SOS2):c.3088A>G (p.Thr1030Ala)	rs550680554	0.00010
NM_006939.4(SOS2):c.2261G>A (p.Ser754Asn)	rs181275468	0.00002
NM_006939.4(SOS2):c.1339C>A (p.Pro447Thr)	rs2502991376
NM_006939.4(SOS2):c.584G>C (p.Gly195Ala)	rs1595007024
NM_006939.4(SOS2):c.709C>A (p.Pro237Thr)	rs758433120

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