List of variants in gene CRX reported as likely pathogenic by Institute of Human Genetics, Univ. Regensburg, Univ. Regensburg

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000554.6(CRX):c.206G>A (p.Arg69His)	rs775073228	0.00002
NM_000554.6(CRX):c.121C>T (p.Arg41Trp)	rs104894672	0.00001
NM_000554.6(CRX):c.122G>C (p.Arg41Pro)
NM_000554.6(CRX):c.158A>G (p.Glu53Gly)

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