List of variants in gene TTI2 reported as uncertain significance by Genetic Services Laboratory, University of Chicago

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001102401.4(TTI2):c.1063C>T (p.Arg355Cys)	rs138108276	0.00392
NM_001102401.4(TTI2):c.1115+7C>G	rs199720231	0.00194
NM_001102401.4(TTI2):c.1135C>T (p.Arg379Trp)	rs140977711	0.00006
NM_001102401.4(TTI2):c.695C>T (p.Thr232Ile)	rs369757546	0.00006
NM_001102401.4(TTI2):c.934C>T (p.Leu312Phe)	rs776062163	0.00001
NM_001102401.4(TTI2):c.489del (p.Pro162_Trp163insTer)	rs749233205
NM_001102401.4(TTI2):c.980A>G (p.His327Arg)	rs1554527020
NM_001102401.4(TTI2):c.98T>G (p.Ile33Ser)	rs930230508

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