ClinVar Miner

List of variants reported as pathogenic for ATTRV122I amyloidosis by Amyloidosis Center, Boston University School of Medicine

Included ClinVar conditions (5):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000371.4(TTR):c.212_217dup (p.Glu71_Ser72dup)	rs1555631390
NM_000371.4(TTR):c.[239C>T];[424G>A]

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