ClinVar Miner

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

Included ClinVar conditions (322):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
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HGVS dbSNP gnomAD frequency
NM_016356.5(DCDC2):c.426-13C>T rs807703 0.98337
NM_016356.5(DCDC2):c.*3C>G rs9358755 0.72045
NM_016356.5(DCDC2):c.661A>G (p.Ser221Gly) rs2274305 0.51051
NM_016356.5(DCDC2):c.1368A>T (p.Lys456Asn) rs9460973 0.15425
NM_016356.5(DCDC2):c.1017C>T (p.Val339=) rs9467075 0.13584
NM_016356.5(DCDC2):c.454C>G (p.Pro152Ala) rs33914824 0.03882
NM_016356.5(DCDC2):c.1044C>T (p.Asp348=) rs143313706 0.00286
NM_016356.5(DCDC2):c.425+14C>A rs77544788 0.00279
NM_016356.5(DCDC2):c.855A>G (p.Ser285=) rs141519329 0.00249
NM_016356.5(DCDC2):c.478A>C (p.Arg160=) rs201204772 0.00030
NM_016356.5(DCDC2):c.294-21GTTT[2] rs374485384
NM_016356.5(DCDC2):c.349-16dup rs746353912

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