ClinVar Miner

List of variants reported as likely pathogenic for Corneal dystrophy

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Total variants: 4
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HGVS dbSNP
NM_000358.3(TGFBI):c.1501C>A (p.Pro501Thr) rs121909212
NM_024915.3(GRHL2):c.20+257delT rs1554579832
NM_024915.4(GRHL2):c.20+133del rs1554579819
NM_024915.4(GRHL2):c.20+544G>T rs1554579878

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