List of variants in gene RPGRIP1 reported as uncertain significance by Breakthrough Genomics, Breakthrough Genomics

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_020366.4(RPGRIP1):c.2665G>A (p.Ala889Thr)	rs184926375	0.00031
NM_020366.4(RPGRIP1):c.2794C>G (p.Pro932Ala)	rs773491339	0.00005
NM_020366.4(RPGRIP1):c.1059G>C (p.Leu353Phe)	rs756365691	0.00002
NM_020366.4(RPGRIP1):c.3773C>T (p.Thr1258Ile)	rs759191514	0.00001
NM_020366.4(RPGRIP1):c.155G>A (p.Arg52Gln)	rs374171080

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