List of variants in gene COL5A2 reported as uncertain significance for hematologic disorder

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000393.5(COL5A2):c.4067A>G (p.Asp1356Gly)	rs140952583	0.00036
NM_000393.5(COL5A2):c.2786C>T (p.Ala929Val)	rs747843876	0.00001

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