ClinVar Miner

List of variants in gene RXYLT1 reported as likely benign for congenital vitreoretinal dysplasia

Included ClinVar conditions (42):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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NM_014254.3(RXYLT1):c.126C>G (p.Gly42=) rs760389276
NM_014254.3(RXYLT1):c.1272G>A (p.Glu424=) rs536862073
NM_014254.3(RXYLT1):c.144C>G (p.Ala48=) rs1407024718
NM_014254.3(RXYLT1):c.373G>C (p.Asp125His) rs188655071
NM_014254.3(RXYLT1):c.43C>T (p.Leu15=) rs770861350

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