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

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NC_000012.12:g.6867521G>A	rs1800201	0.03488
NM_000365.6(TPI1):c.*549A>G	rs114310136	0.00243
NM_000365.6(TPI1):c.366C>T (p.Leu122=)	rs138131191	0.00081
NM_000365.6(TPI1):c.-31C>T	rs200692430	0.00076
NM_000365.6(TPI1):c.*178G>A	rs144171030	0.00018
NM_000365.6(TPI1):c.*519T>C	rs377186570	0.00008
NM_000365.6(TPI1):c.690C>T (p.Phe230=)	rs782267337	0.00004
NM_000365.6(TPI1):c.116-13A>G	rs782238701	0.00002
NM_000365.6(TPI1):c.543+5C>G	rs782153322	0.00002
NM_000365.6(TPI1):c.457+7C>G

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