List of variants in gene TNK2 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001382273.1(TNK2):c.84T>C (p.Asp28=)	rs3747669	0.39209
NM_001382273.1(TNK2):c.2219C>T (p.Pro740Leu)	rs56260729	0.16426
NM_001382273.1(TNK2):c.2364T>C (p.Ala788=)	rs1056749	0.15569
NM_001382273.1(TNK2):c.2115G>A (p.Pro705=)	rs7516	0.10655
NM_001382273.1(TNK2):c.1764C>T (p.Phe588=)	rs1056726	0.06127
NM_001382273.1(TNK2):c.3164G>A (p.Arg1055His)	rs13433937	0.03524
NM_001382273.1(TNK2):c.915C>T (p.Arg305=)	rs3761718	0.01476
NM_001382273.1(TNK2):c.351C>T (p.Leu117=)	rs56003471	0.01208
NM_001382273.1(TNK2):c.2675G>A (p.Arg892His)	rs112384084	0.01127
NM_001382273.1(TNK2):c.-18-6C>T	rs113106902
NM_001382273.1(TNK2):c.2078G>A (p.Arg693Gln)
NM_001382273.1(TNK2):c.2287C>T (p.Arg763Trp)

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