List of variants in gene SH2D1A reported as uncertain significance for autoinflammatory syndrome

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_002351.5(SH2D1A):c.273T>C (p.Asp91=)	rs775759946	0.00001
NM_002351.5(SH2D1A):c.7G>T (p.Ala3Ser)	rs148554414	0.00001

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