List of variants in gene RPGRIP1 reported as uncertain significance by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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.840G>C (p.Lys280Asn)	rs1208451312
NM_020366.4(RPGRIP1):c.94A>G (p.Met32Val)	rs2139144559
NM_020366.4(RPGRIP1):c.953C>G (p.Ala318Gly)	rs1325466987

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