List of variants in gene TTC8 reported as benign by PreventionGenetics, part of Exact Sciences

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.329+48T>C	rs17700296	0.19562
NM_144596.4(TTC8):c.1432-12T>C	rs79747892	0.03653
NM_144596.4(TTC8):c.625-5C>T	rs137853922	0.00807
NM_144596.4(TTC8):c.194A>G (p.Asp65Gly)	rs114557412	0.00354
NM_144596.4(TTC8):c.1401G>A (p.Pro467=)	rs114064158	0.00319
NM_144596.4(TTC8):c.-25G>A	rs7145692	0.00290
NM_144596.4(TTC8):c.284A>G (p.Lys95Arg)	rs150880478	0.00272
NM_144596.4(TTC8):c.299A>G (p.Asn100Ser)	rs139392523	0.00230

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