List of variants in gene RP2 reported as likely benign 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_006915.3(RP2):c.260C>T (p.Thr87Ile)	rs147783915	0.00496
NM_006915.3(RP2):c.1001C>A (p.Ser334Tyr)	rs139796627	0.00021
NM_006915.3(RP2):c.814A>G (p.Met272Val)	rs143606776	0.00011
NM_006915.3(RP2):c.751A>G (p.Arg251Gly)	rs190443020	0.00009
NM_006915.3(RP2):c.*1696ATT[9]	rs782229405
NM_006915.3(RP2):c.1696_1697insGTATTA	rs1556328727
NM_006915.3(RP2):c.*808del	rs781852469

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