ClinVar Miner

List of variants in gene CNP, LOC130060859 studied for myopia 2, autosomal dominant

Included ClinVar conditions (1):

Myopia 2, autosomal dominant

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_033133.5(CNP):c.-67C>T	rs1422332023	0.00001
NM_033133.5(CNP):c.-77C>T	rs1387950081

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