ClinVar Miner

List of variants in gene CRX reported as pathogenic for not provided

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Total variants: 6
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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.239A>C (p.Glu80Ala) rs104894671
NM_000554.6(CRX):c.448del (p.Ser150fs) rs886044121
NM_000554.6(CRX):c.501dup (p.Glu168fs) rs1968166700
NM_000554.6(CRX):c.650del (p.Gly217fs) rs281865517

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