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

Submission 1 (benign) minimum review status:		Submission 1 (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: 4

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HGVS	dbSNP	gnomAD frequency
NM_032977.4(CASP10):c.1216A>T (p.Ile406Leu)	rs80358239	0.00340
NM_032977.4(CASP10):c.1502C>T (p.Pro501Leu)	rs148939095	0.00091
NM_032977.4(CASP10):c.20A>G (p.His7Arg)	rs200935960	0.00004
NM_032977.4(CASP10):c.49A>G (p.Lys17Glu)	rs552561721	0.00001

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