List of variants in gene TTC8 reported as likely benign by Fulgent Genetics, Fulgent Genetics

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_144596.4(TTC8):c.910-16T>G	rs199763558	0.00053
NM_144596.4(TTC8):c.909+18T>C	rs111707320	0.00024
NM_144596.4(TTC8):c.1347+18G>A	rs368504643	0.00008
NM_144596.4(TTC8):c.54G>A (p.Arg18=)	rs745942356	0.00003
NM_144596.4(TTC8):c.114+12C>A	rs372634452	0.00001
NM_144596.4(TTC8):c.711-16A>C	rs747396066	0.00001
NM_144596.4(TTC8):c.1464G>A (p.Ala488=)	rs142073418
NM_144596.4(TTC8):c.324C>T (p.Ala108=)	rs571883979

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