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

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001206744.2(TPO):c.1193G>C (p.Ser398Thr)	rs2175977	0.65696
NM_001206744.2(TPO):c.2540T>C (p.Val847Ala)	rs1126799	0.62508
NM_001206744.2(TPO):c.2173A>C (p.Thr725Pro)	rs732609	0.46998
NM_001206744.2(TPO):c.1117G>T (p.Ala373Ser)	rs2280132	0.43513
NM_001206744.2(TPO):c.2145C>T (p.Pro715=)	rs732608	0.41037
NM_001206744.2(TPO):c.1998C>T (p.Asp666=)	rs1126797	0.35994
NM_001206744.2(TPO):c.2006+20G>A	rs10189329	0.08761
NM_001206744.2(TPO):c.2387-17C>T	rs28912996	0.00286
NM_001206744.2(TPO):c.2242G>A (p.Val748Met)	rs28991292	0.00197
NM_001206744.2(TPO):c.12C>G (p.Leu4=)	rs9678281
NM_001206744.2(TPO):c.769G>T (p.Ala257Ser)	rs4927611

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