List of variants in gene combination LOC130008356, POC1B, POC1B-GALNT4 reported as uncertain significance for Cone-rod dystrophy 20

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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_172240.3(POC1B):c.46G>A (p.Gly16Ser)	rs780295968	0.00001
NM_172240.3(POC1B):c.47G>T (p.Gly16Val)
NM_172240.3(POC1B):c.76C>G (p.Leu26Val)
NM_172240.3(POC1B):c.88G>A (p.Gly30Ser)	rs1456154895

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