List of variants in gene combination LOC130068202, RP2 reported as uncertain significance for Retinitis pigmentosa

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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_006915.3(RP2):c.-35A>G	rs909119773	0.00003
NM_006915.3(RP2):c.-26G>T	rs782652659	0.00002
NM_006915.3(RP2):c.11T>G (p.Phe4Cys)	rs782190396	0.00002

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