Variants in gene COL1A2 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000089.4(COL1A2):c.2755G>A (p.Gly919Ser)	rs749621872	0.00002
NM_000089.4(COL1A2):c.2701G>A (p.Gly901Ser)	rs72659306	0.00001
NM_000089.4(COL1A2):c.838G>A (p.Gly280Ser)	rs72656387	0.00001
NM_000089.4(COL1A2):c.1072G>A (p.Gly358Ser)	rs66619856
NM_000089.4(COL1A2):c.1342G>C (p.Gly448Arg)	rs1584320605
NM_000089.4(COL1A2):c.1541G>C (p.Gly514Ala)	rs1791962073
NM_000089.4(COL1A2):c.1576G>A (p.Gly526Arg)	rs72658129
NM_000089.4(COL1A2):c.2233G>A (p.Gly745Arg)
NM_000089.4(COL1A2):c.2864G>A (p.Gly955Asp)	rs2115952213
NM_000089.4(COL1A2):c.2965_2973dup (p.Pro989_Gly991dup)	rs1554398396
NM_000089.4(COL1A2):c.2989G>A (p.Gly997Ser)	rs1562907287
NM_000089.4(COL1A2):c.964G>A (p.Gly322Ser)	rs72656394

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