List of variants in gene combination GRM6, ZNF454 reported as likely pathogenic for congenital stationary night blindness 1B

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000843.4(GRM6):c.2066del (p.Pro689fs)	rs755967391
NM_000843.4(GRM6):c.2236_2237del (p.Met746fs)
NM_000843.4(GRM6):c.2560C>T (p.Arg854Ter)

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