ClinVar Miner

List of variants in gene TTR reported as affects for hyperthyroxinemia

Included ClinVar conditions (4):

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000371.4(TTR):c.385G>A (p.Ala129Thr)	rs267607159	0.00005
NM_000371.4(TTR):c.386C>T (p.Ala129Val)	rs121918092	0.00004

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