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: 2

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HGVS	dbSNP
NM_015272.5(RPGRIP1L):c.2200C>T (p.Arg734Ter)	rs751128300
NM_015272.5(RPGRIP1L):c.2614C>T (p.Gln872Ter)	rs121918203

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