List of variants in gene TPI1 reported as likely pathogenic for hematologic disorder

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_000365.6(TPI1):c.315G>C (p.Glu105Asp)	rs121964845	0.00012
NM_000365.6(TPI1):c.32del (p.Gly11fs)
NM_000365.6(TPI1):c.544-1G>C	rs2138094606

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