Variants in gene COL11A2 with conflicting interpretations "pathogenic" and "likely pathogenic"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) 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: 2

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HGVS	dbSNP
NM_080680.3(COL11A2):c.3100C>T (p.Arg1034Cys)	rs121912947
NM_080680.3(COL11A2):c.966dup (p.Thr323fs)	rs748440351

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