Variants in gene RPGRIP1L with conflicting interpretations "pathogenic" and "likely pathogenic"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 8

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HGVS	dbSNP	gnomAD frequency
NM_015272.5(RPGRIP1L):c.2614C>T (p.Gln872Ter)	rs121918203	0.00005
NM_015272.5(RPGRIP1L):c.2050C>T (p.Gln684Ter)	rs121918204	0.00002
NM_015272.5(RPGRIP1L):c.3529C>T (p.Arg1177Ter)	rs778533826	0.00002
NM_015272.5(RPGRIP1L):c.1372G>T (p.Glu458Ter)	rs776941281	0.00001
NM_015272.5(RPGRIP1L):c.1489G>T (p.Glu497Ter)	rs756821449	0.00001
NM_015272.5(RPGRIP1L):c.196C>T (p.Gln66Ter)	rs751444506	0.00001
NM_015272.5(RPGRIP1L):c.2299C>T (p.Gln767Ter)	rs1326042797	0.00001
NM_015272.5(RPGRIP1L):c.2125C>T (p.Arg709Ter)	rs1037406858

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