List of variants in gene RP1L1 reported as pathogenic for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_178857.6(RP1L1):c.1107G>A (p.Trp369Ter)	rs567106336	0.00002
NM_178857.6(RP1L1):c.1122G>A (p.Trp374Ter)	rs1205382497	0.00001
NM_178857.6(RP1L1):c.133C>T (p.Arg45Trp)	rs267607017	0.00001
NM_178857.6(RP1L1):c.2107C>T (p.Arg703Ter)	rs775708703

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