ClinVar Miner

List of variants in gene DOK1, LOXL3 studied for myopia 28, autosomal recessive

Included ClinVar conditions (1):

Myopia 28, autosomal recessive

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_032603.5(LOXL3):c.39dup (p.Leu14fs)	rs35904632
NM_032603.5(LOXL3):c.449delinsAA (p.Pro150fs)
NM_032603.5(LOXL3):c.594del (p.Gln199fs)	rs2104441352

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