List of variants in gene combination CRYGD, LOC100507443 reported as pathogenic for cataract

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_006891.4(CRYGD):c.109C>A (p.Arg37Ser)	rs121909597
NM_006891.4(CRYGD):c.176G>A (p.Arg59His)	rs121909596
NM_006891.4(CRYGD):c.402C>A (p.Tyr134Ter)	rs398122948
NM_006891.4(CRYGD):c.418C>T (p.Arg140Ter)	rs1337897299
NM_006891.4(CRYGD):c.43C>T (p.Arg15Cys)	rs121909595
NM_006891.4(CRYGD):c.470G>A (p.Trp157Ter)	rs121909598
NM_006891.4(CRYGD):c.70C>A (p.Pro24Thr)	rs28931605
NM_006891.4(CRYGD):c.70C>T (p.Pro24Ser)	rs28931605

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