List of variants in gene TTC21B reported as likely benign for Connective tissue disorder

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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_024753.5(TTC21B):c.838A>G (p.Met280Val)	rs112868646	0.01295
NM_024753.5(TTC21B):c.665A>T (p.Gln222Leu)	rs80026831	0.01209
NM_024753.5(TTC21B):c.1965G>A (p.Arg655=)	rs16822802	0.00754
NM_024753.5(TTC21B):c.3004C>G (p.Leu1002Val)	rs146496725	0.00517
NM_024753.5(TTC21B):c.3416T>C (p.Val1139Ala)	rs149454830	0.00267
NM_024753.5(TTC21B):c.114C>G (p.Val38=)	rs34486024
NM_024753.5(TTC21B):c.2569-10dup	rs144600502
NM_024753.5(TTC21B):c.3519T>G (p.Thr1173=)	rs115504901

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