List of variants in gene RPGRIP1 reported as likely benign by Ambry Genetics

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_020366.4(RPGRIP1):c.2332G>A (p.Asp778Asn)	rs768913743	0.00005
NM_020366.4(RPGRIP1):c.2099G>A (p.Arg700Gln)	rs768190736	0.00001
NM_020366.4(RPGRIP1):c.110C>A (p.Pro37His)	rs749943816
NM_020366.4(RPGRIP1):c.29G>A (p.Gly10Glu)	rs756665749
NM_020366.4(RPGRIP1):c.301G>A (p.Ala101Thr)
NM_020366.4(RPGRIP1):c.3133A>G (p.Thr1045Ala)

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