List of variants in gene TTR reported as likely pathogenic by GeneDx

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000371.4(TTR):c.262A>T (p.Ile88Leu)	rs121918085	0.00004
NM_000371.4(TTR):c.293A>T (p.Tyr98Phe)	rs958191819	0.00001
NM_000371.4(TTR):c.220_221inv (p.Glu74Ser)
NM_000371.4(TTR):c.236C>A (p.Thr79Lys)	rs730881163
NM_000371.4(TTR):c.252T>G (p.Phe84Leu)	rs2073510805
NM_000371.4(TTR):c.260G>A (p.Gly87Glu)

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