ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
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NM_002485.4(NBN):c.1125-2A>G rs1554559373
NM_002485.4(NBN):c.1397+1_1397+9delinsACA rs876659666
NM_002485.4(NBN):c.163_171+3del rs1057516772
NM_002485.4(NBN):c.2071-1G>A rs786201965
NM_002485.4(NBN):c.320+2T>G rs1563580433
NM_002485.4(NBN):c.37+1G>A rs574673404
NM_002485.4(NBN):c.481-2A>T rs751567476
NM_002485.4(NBN):c.7A>T (p.Lys3Ter) rs779098734
NM_002485.4(NBN):c.896+1G>A rs778306619
NM_002485.4(NBN):c.896+1G>T rs778306619
NM_002485.4(NBN):c.995-2A>G rs876659521

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