List of variants in gene TTC21B reported as likely benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_024753.5(TTC21B):c.3004C>G (p.Leu1002Val)	rs146496725	0.00537
NM_024753.5(TTC21B):c.724G>A (p.Asp242Asn)	rs74447004	0.00356
NM_024753.5(TTC21B):c.3416T>C (p.Val1139Ala)	rs149454830	0.00267
NM_024753.5(TTC21B):c.2472G>A (p.Leu824=)	rs114725374	0.00107
NM_024753.5(TTC21B):c.3874-14T>C	rs200347449	0.00096
NM_024753.5(TTC21B):c.1650A>G (p.Glu550=)	rs145926679	0.00050
NM_024753.5(TTC21B):c.3552G>A (p.Ala1184=)	rs148113339	0.00008
NM_024753.5(TTC21B):c.843A>G (p.Glu281=)	rs201311475	0.00001
NM_024753.5(TTC21B):c.1956A>G (p.Glu652=)	rs1686129480

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