List of variants in gene combination HMCN1, LOC126805953 reported as uncertain significance for age-related macular degeneration

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_031935.3(HMCN1):c.16460G>A (p.Arg5487His)	rs184128357	0.00047
NM_031935.3(HMCN1):c.16526G>A (p.Arg5509Gln)	rs140641844	0.00010

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