List of variants in gene COL1A2 reported as uncertain significance for Ehlers-Danlos syndrome, arthrochalasia type

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000089.4(COL1A2):c.1252-6del	rs886062516
NM_000089.4(COL1A2):c.3226C>T (p.Pro1076Ser)	rs763974489
NM_000089.4(COL1A2):c.71C>G (p.Ser24Cys)	rs763546006

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