Variants in gene TTC21B with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_024753.5(TTC21B):c.3004C>G (p.Leu1002Val)	rs146496725	0.00517
NM_024753.5(TTC21B):c.1846C>T (p.Arg616Cys)	rs139441507	0.00279
NM_024753.5(TTC21B):c.1676T>G (p.Val559Gly)	rs149325238	0.00190
NM_024753.5(TTC21B):c.863T>C (p.Phe288Ser)	rs761856542	0.00005

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