ClinVar Miner

List of variants in gene DCDC2 reported as likely benign for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
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HGVS dbSNP
NM_016356.5(DCDC2):c.1099T>A (p.Ser367Thr)
NM_016356.5(DCDC2):c.1208G>A (p.Arg403His) rs139858268
NM_016356.5(DCDC2):c.349-9C>G rs765613994
NM_016356.5(DCDC2):c.471T>G (p.Leu157=)
NM_016356.5(DCDC2):c.543C>A (p.Ser181Arg) rs141060456
NM_016356.5(DCDC2):c.543C>T (p.Ser181=) rs141060456
NM_016356.5(DCDC2):c.705-4A>C
NM_016356.5(DCDC2):c.715T>G (p.Ser239Ala) rs144695853
NM_016356.5(DCDC2):c.750T>G (p.Ser250=) rs372157851

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