Variants in gene COL11A1 with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001854.4(COL11A1):c.1245+1G>A	rs766849561	0.00005
NM_001854.4(COL11A1):c.1003G>T (p.Glu335Ter)	rs776004614	0.00001
NM_001854.4(COL11A1):c.2513G>A (p.Gly838Glu)	rs372419698	0.00001
NM_001854.4(COL11A1):c.1190dup (p.Pro397_Asn398insTer)	rs1343199316
NM_001854.4(COL11A1):c.1630-2del	rs1057517989
NM_001854.4(COL11A1):c.2916+1G>A	rs2101595036
NM_001854.4(COL11A1):c.3717del (p.Gly1240fs)	rs2101066868
NM_001854.4(COL11A1):c.4554+1G>C	rs886044244
NM_001854.4(COL11A1):c.484G>A (p.Gly162Arg)	rs1672165764

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