List of variants in gene SPP2 reported as likely benign for inherited retinal dystrophy

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_006944.3(SPP2):c.173C>T (p.Pro58Leu)	rs143082886	0.00005
NM_006944.3(SPP2):c.105C>T (p.Tyr35=)	rs753888543	0.00002

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