ClinVar Miner

List of variants in gene DCN reported as likely benign for corneal dystrophy

Included ClinVar conditions (45):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
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HGVS dbSNP gnomAD frequency
NM_001920.4(DCN):c.-325A>G rs147956869 0.00432
NM_001920.4(DCN):c.-249A>G rs189853358 0.00078
NM_001920.5(DCN):c.54G>A (p.Pro18=) rs145597441 0.00029
NM_001920.5(DCN):c.621T>G (p.Ile207Met) rs373676217 0.00014
NM_001920.4(DCN):c.-296C>T rs540013218 0.00004
NM_001920.5(DCN):c.879C>T (p.Tyr293=) rs144307891 0.00004
NM_001920.5(DCN):c.944C>A (p.Pro315His) rs777270608 0.00004
NM_001920.5(DCN):c.1066G>A (p.Gly356Arg) rs775666283 0.00002
NM_001920.5(DCN):c.555G>T (p.Pro185=) rs147765043

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