List of variants in gene TRIT1 reported as likely benign by GeneDx

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_017646.6(TRIT1):c.316-294A>G	rs11580351	0.01673
NM_017646.6(TRIT1):c.1007-233G>T	rs115570662	0.01246
NM_017646.6(TRIT1):c.1235-195A>C	rs114327070	0.00639
NM_017646.6(TRIT1):c.415-319T>C	rs114806141	0.00447
NM_017646.6(TRIT1):c.174+255G>A	rs149708820	0.00419
NM_017646.6(TRIT1):c.1006+291G>C	rs147493574	0.00353
NM_017646.6(TRIT1):c.633T>C (p.Gly211=)	rs1039399054	0.00003
NM_017646.6(TRIT1):c.704-271AT[3]	rs555291147

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