ClinVar Miner

List of variants in gene NBN reported as likely pathogenic by Mendelics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_002485.5(NBN):c.702+1del rs1586088347
NM_002485.5(NBN):c.89del (p.Asn30fs) rs587781718

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