Variants in gene CASP10 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_032977.4(CASP10):c.1216A>T (p.Ile406Leu)	rs80358239	0.00307
NM_032977.4(CASP10):c.913A>G (p.Lys305Glu)	rs149912574	0.00015
NM_032977.4(CASP10):c.1297G>A (p.Glu433Lys)	rs200540853	0.00014
NM_032977.4(CASP10):c.1466G>A (p.Arg489Gln)	rs535121774	0.00004
NM_032977.4(CASP10):c.879C>A (p.Ser293Arg)	rs369897442	0.00003
NM_032977.4(CASP10):c.442-14T>G	rs755555484	0.00001
NM_032977.4(CASP10):c.81T>C (p.Ile27=)	rs751728796	0.00001
NM_032977.4(CASP10):c.534A>G (p.Val178=)	rs146233833

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