ClinVar Miner

List of variants reported as likely pathogenic for corneal disorder by DBGen Ocular Genomics

Included ClinVar conditions (75):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_000223.4(KRT12):c.1181T>C (p.Leu394Pro)
NM_057088.3(KRT3):c.1492G>A (p.Glu498Lys) rs2121217835
NM_057088.3(KRT3):c.1527G>T (p.Glu509Asp)

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