List of variants in gene RPGR reported as likely benign for not specified

Minimum submission review status:		Collection method:
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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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001034853.2(RPGR):c.1697G>A (p.Gly566Glu)	rs1801688	0.09526
NM_001034853.2(RPGR):c.1274G>A (p.Arg425Lys)	rs1801687	0.09261
NM_001034853.2(RPGR):c.620-41T>C	rs45486397	0.03373
NM_001034853.2(RPGR):c.223A>G (p.Ile75Val)	rs111631988	0.03363
NM_001034853.2(RPGR):c.3231T>A (p.Asn1077Lys)	rs62636730	0.02044
NM_001034853.2(RPGR):c.1598C>T (p.Thr533Met)	rs41312104	0.02014
NM_001034853.2(RPGR):c.1059+6G>A	rs377731326	0.00035
NM_001034853.2(RPGR):c.141T>G (p.Ser47=)	rs62638631	0.00034
NM_001034853.2(RPGR):c.1245+6A>G	rs886038281	0.00005
NM_001034853.2(RPGR):c.1200T>C (p.Asn400=)	rs768625051	0.00001
NM_000328.3(RPGR):c.2267C>T (p.Ser756Leu)	rs766828733
NM_001034853.2(RPGR):c.1084G>A (p.Val362Ile)	rs866718135
NM_001034853.2(RPGR):c.155-13del	rs886038282
NM_001034853.2(RPGR):c.2520GGAGGGGGAAGAGGAGGAAGG[3] (p.829EEEEGEG[5])	rs751710678
NM_001034853.2(RPGR):c.2541G>A (p.Gly847=)	rs750364695

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