List of variants in gene TTC21B reported as likely pathogenic for not provided

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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_024753.5(TTC21B):c.626C>T (p.Pro209Leu)	rs140511594	0.00011
NM_024753.5(TTC21B):c.2500C>T (p.Gln834Ter)	rs79746977	0.00009
NM_024753.5(TTC21B):c.2209G>T (p.Glu737Ter)	rs748663904	0.00004
NM_024753.5(TTC21B):c.1715C>A (p.Ser572Ter)	rs369159801	0.00002
NM_024753.5(TTC21B):c.2741del (p.Cys914fs)	rs754911118	0.00002
NM_024753.5(TTC21B):c.1088-1G>C	rs753627675	0.00001
NM_024753.5(TTC21B):c.553-2A>G	rs773580610	0.00001
NM_024753.5(TTC21B):c.3383_3402del (p.Tyr1128fs)	rs1685077018
NM_024753.5(TTC21B):c.3806-2A>G	rs2105275776

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