ClinVar Miner

List of variants in gene DCN reported as uncertain significance for corneal disorder

Included ClinVar conditions (70):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_001920.5(DCN):c.*148T>G rs564091657 0.00091
NM_001920.5(DCN):c.*80C>T rs531541570 0.00016
NM_001920.5(DCN):c.621T>G (p.Ile207Met) rs373676217 0.00014
NM_001920.5(DCN):c.-180A>T rs757178906 0.00009
NM_001920.4(DCN):c.-307A>G rs886049891 0.00008
NM_001920.5(DCN):c.-187A>G rs551534809 0.00006
NM_001920.5(DCN):c.*354A>G rs778805558 0.00005
NM_001920.5(DCN):c.*220G>C rs886049890 0.00004
NM_001920.5(DCN):c.210G>A (p.Leu70=) rs200516355 0.00003
NM_001920.5(DCN):c.632A>G (p.Asn211Ser) rs758510607 0.00002
NM_001920.5(DCN):c.*351T>C rs1201458812 0.00001
NM_001920.5(DCN):c.*566T>A rs1449263175 0.00001
NM_001920.5(DCN):c.560A>G (p.Lys187Arg) rs555705830 0.00001
NM_001920.5(DCN):c.*289A>T rs886049889
NM_001920.5(DCN):c.*341A>G rs1880967544
NM_001920.5(DCN):c.*443T>G rs886049888
NM_001920.5(DCN):c.1062A>T (p.Gln354His) rs765239185
NM_001920.5(DCN):c.127G>A (p.Asp43Asn) rs1883428257
NM_001920.5(DCN):c.47_50del (p.Ala16fs) rs1565791154

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