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

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_005633.4(SOS1):c.2105A>G (p.Tyr702Cys)	rs757094189	0.00001
NM_005633.4(SOS1):c.571G>A (p.Glu191Lys)	rs886041241	0.00001
NM_005633.4(SOS1):c.1433C>G (p.Pro478Arg)	rs1553356111
NM_005633.4(SOS1):c.1646C>A (p.Thr549Lys)	rs730881046
NM_005633.4(SOS1):c.2671G>A (p.Glu891Lys)	rs1553353452
NM_005633.4(SOS1):c.323A>G (p.Glu108Gly)	rs886041923

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