List of variants in gene OCA2 reported as likely pathogenic for Albinism

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: 4

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HGVS	dbSNP
NM_000275.3(OCA2):c.1025A>G (p.Tyr342Cys)	rs142931246
NM_000275.3(OCA2):c.1660T>C (p.Trp554Arg)	rs1384042381
NM_000275.3(OCA2):c.2339G>A (p.Gly780Asp)	rs141949212
NM_000275.3(OCA2):c.646+1825_807+679del

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