C1855305[trait identifier] AND "Mayo Clinic Laboratories, Mayo Clinic" - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 547887	NM_001017995.3(SH3PXD2B):c.1403G>A (p.Arg468Gln)	SH3PXD2B (R468Q)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 352817	NM_001017995.3(SH3PXD2B):c.997G>A (p.Gly333Ser)	SH3PXD2B (G333S)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity