List of variants in gene RP2 reported as uncertain significance for RPGR-related retinopathy

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_006915.2(RP2):c.-97C>T	rs975776959	0.00015
NM_006915.3(RP2):c.650A>G (p.Asn217Ser)	rs781878275	0.00007
NM_006915.2(RP2):c.-70A>G	rs1057515891	0.00003
NM_006915.3(RP2):c.243_246del	rs782684761
NM_006915.3(RP2):c.884-14G>A	rs1602354996

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