List of variants in gene combination CERKL, LOC129935215 reported as likely pathogenic for retinitis pigmentosa

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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_201548.5(CERKL):c.2T>G (p.Met1Arg)	rs1187991259	0.00001
NM_201548.5(CERKL):c.2T>C (p.Met1Thr)	rs1187991259
NM_201548.5(CERKL):c.6del (p.Trp3fs)
NM_201548.5(CERKL):c.8G>A (p.Trp3Ter)	rs2105569550

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