List of variants in gene SH2B3 reported as uncertain significance for Primary familial polycythemia due to EPO receptor mutation; Thrombocythemia 1; Primary myelofibrosis

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_005475.3(SH2B3):c.1198G>A (p.Glu400Lys)	rs72650673	0.00080
NM_005475.3(SH2B3):c.1183G>A (p.Glu395Lys)	rs148636776	0.00023
NM_005475.3(SH2B3):c.1696C>T (p.Arg566Trp)

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