List of variants in gene TPO reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001206744.2(TPO):c.1813A>T (p.Thr605Ser)	rs61748996	0.00210
NM_001206744.2(TPO):c.2541G>A (p.Val847=)	rs61734476	0.00183
NM_001206744.2(TPO):c.978G>A (p.Ala326=)	rs145985334	0.00114
NM_001206744.2(TPO):c.2499C>T (p.Asp833=)	rs142148533	0.00083
NM_001206744.2(TPO):c.660C>T (p.Val220=)	rs151154074	0.00076
NM_001206744.2(TPO):c.404C>A (p.Pro135His)	rs61758083	0.00034
NM_001206744.2(TPO):c.501C>T (p.Gly167=)	rs370072872	0.00015
NM_001206744.2(TPO):c.348G>A (p.Thr116=)	rs374499898	0.00001
NM_001206744.2(TPO):c.1683G>T (p.Thr561=)	rs748083838
NM_001206744.2(TPO):c.1857C>G (p.Ala619=)	rs140322336
NM_001206744.2(TPO):c.2523C>T (p.Ser841=)
NM_001206744.2(TPO):c.342T>C (p.His114=)
NM_001206744.2(TPO):c.954C>T (p.Asn318=)

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