List of variants in gene RPGRIP1 reported as likely benign by Clinical Genetics, Academic Medical Center

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_020366.4(RPGRIP1):c.2284C>T (p.Leu762=)	rs145896974	0.00240
NM_020366.4(RPGRIP1):c.1753C>T (p.Pro585Ser)	rs147586703	0.00155
NM_020366.4(RPGRIP1):c.2711-13G>T	rs369991630	0.00026

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