List of variants in gene TTC19 reported as likely 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_017775.4(TTC19):c.583C>T (p.Gln195Ter)	rs764720544	0.00004
NM_017775.4(TTC19):c.423+1G>C	rs781491387	0.00001
NM_017775.4(TTC19):c.424-1G>A
NM_017775.4(TTC19):c.520-2A>G
NM_017775.4(TTC19):c.581+1G>C

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