List of variants in gene CRX reported as likely benign for not provided

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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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000554.6(CRX):c.365G>A (p.Gly122Asp)	rs61748441	0.00614
NM_000554.6(CRX):c.196G>A (p.Val66Ile)	rs61748438	0.00231
NM_000554.6(CRX):c.253-15G>A	rs145805694	0.00187
NM_000554.6(CRX):c.28C>G (p.His10Asp)	rs139340178	0.00060
NM_000554.6(CRX):c.425A>G (p.Tyr142Cys)	rs61748442	0.00032
NM_000554.6(CRX):c.-29T>A	rs1568624071
NM_000554.6(CRX):c.531T>C (p.Ala177=)
NM_000554.6(CRX):c.570C>A (p.Pro190=)	rs1599991852
NM_000554.6(CRX):c.723C>T (p.Ser241=)	rs770257260
NM_000554.6(CRX):c.879C>G (p.Ala293=)

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