List of variants in gene CACNA1F reported as likely benign for CACNA1F-related retinopathy

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001256789.3(CACNA1F):c.1523G>A (p.Arg508Gln)	rs34162630	0.01756
NM_001256789.3(CACNA1F):c.2204A>C (p.Asn735Thr)	rs141159097	0.00176
NM_001256789.3(CACNA1F):c.1535G>A (p.Arg512His)	rs146847449
NM_001256789.3(CACNA1F):c.25+1G>A
NM_001256789.3(CACNA1F):c.982A>G (p.Thr328Ala)

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