List of variants in gene combination CERKL, ITGA4 reported as uncertain significance for Retinitis Pigmentosa, Recessive

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_201548.5(CERKL):c.*915C>G	rs116322351	0.02028
NM_201548.5(CERKL):c.*121delinsTGATTTTTCT	rs886055316
NM_201548.5(CERKL):c.1414_1417dup	rs529740971

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