Variants in gene SOS1 with conflicting interpretations "pathogenic" and "likely pathogenic"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 8

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HGVS	dbSNP	gnomAD frequency
NM_005633.4(SOS1):c.1654A>T (p.Arg552Trp)	rs137852814	0.00001
NM_005633.4(SOS1):c.1300G>A (p.Gly434Arg)	rs397517148
NM_005633.4(SOS1):c.1310T>C (p.Ile437Thr)	rs397517150
NM_005633.4(SOS1):c.1655G>T (p.Arg552Met)	rs397517154
NM_005633.4(SOS1):c.2197A>T (p.Ile733Phe)	rs574088829
NM_005633.4(SOS1):c.2207T>G (p.Ile736Arg)	rs1553354396
NM_005633.4(SOS1):c.322G>A (p.Glu108Lys)	rs397517164
NM_005633.4(SOS1):c.508A>G (p.Lys170Glu)	rs397517172

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