Variants in gene TTC21B with conflicting interpretations "uncertain significance" and "likely pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 3

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HGVS	dbSNP	gnomAD frequency
NM_024753.5(TTC21B):c.2014C>T (p.Arg672Trp)	rs140757802	0.00041
NM_024753.5(TTC21B):c.2693G>A (p.Arg898Gln)	rs574017249	0.00006
NM_024753.5(TTC21B):c.1715C>A (p.Ser572Ter)	rs369159801	0.00002

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