List of variants in gene TTI2 reported as likely benign by Breakthrough Genomics, Breakthrough Genomics

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001102401.4(TTI2):c.118C>T (p.Pro40Ser)	rs78781527	0.00501
NM_001102401.4(TTI2):c.581G>C (p.Gly194Ala)	rs186443359	0.00054
NM_001102401.4(TTI2):c.117C>T (p.Arg39=)	rs542413409	0.00006
NM_001102401.4(TTI2):c.276T>C (p.Tyr92=)	rs192489584	0.00002

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