List of variants in gene TTC7A reported as pathogenic for not provided

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_020458.4(TTC7A):c.211G>A (p.Glu71Lys)	rs147914967	0.00003
NM_020458.4(TTC7A):c.1183dup (p.Gln395fs)	rs886042806
NM_020458.4(TTC7A):c.286G>T (p.Glu96Ter)	rs886042805

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