Variants in gene RP1 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: 17

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HGVS	dbSNP	gnomAD frequency
NM_006269.2(RP1):c.1186C>T (p.Arg396Ter)	rs201493928	0.00005
NM_006269.2(RP1):c.515T>G (p.Leu172Arg)	rs180729424	0.00003
NM_006269.2(RP1):c.1498_1499del (p.Met500fs)	rs765129639	0.00002
NM_006269.2(RP1):c.788-2A>T	rs1422250479	0.00001
NM_006269.2(RP1):c.1719_1723del (p.Ser574fs)	rs750542962
NM_006269.2(RP1):c.2025dup (p.Ser676fs)	rs1365669334
NM_006269.2(RP1):c.2035C>T (p.Gln679Ter)	rs104894083
NM_006269.2(RP1):c.2161del (p.Gly723fs)	rs755429480
NM_006269.2(RP1):c.2167G>T (p.Gly723Ter)	rs1585563283
NM_006269.2(RP1):c.2219C>G (p.Ser740Ter)	rs1554519555
NM_006269.2(RP1):c.2296C>T (p.Gln766Ter)	rs775731489
NM_006269.2(RP1):c.2305A>T (p.Lys769Ter)	rs1488237523
NM_006269.2(RP1):c.2391_2392del (p.Arg798_Asp799insTer)
NM_006269.2(RP1):c.2700dup (p.Pro901fs)	rs797044735
NM_006269.2(RP1):c.458dup (p.Arg154fs)	rs781249059
NM_006269.2(RP1):c.668del (p.Gly223fs)	rs1231321479
Single allele

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