ClinVar Miner

List of variants in gene NFKB2 reported as likely benign for agammaglobulinemia

Included ClinVar conditions (31):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
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NM_001077494.3(NFKB2):c.1170C>A (p.Ser390=) rs1200632324
NM_001077494.3(NFKB2):c.1288C>T (p.Pro430Ser) rs202001697
NM_001077494.3(NFKB2):c.1386C>G (p.Leu462=) rs762807587
NM_001077494.3(NFKB2):c.1736G>A (p.Arg579His) rs200227171
NM_001077494.3(NFKB2):c.2072-3C>T rs201550645
NM_001077494.3(NFKB2):c.2167G>A (p.Asp723Asn) rs199577673
NM_001077494.3(NFKB2):c.216G>A (p.Lys72=) rs369551276
NM_001077494.3(NFKB2):c.2286C>T (p.Ser762=) rs899733509
NM_001077494.3(NFKB2):c.2418G>A (p.Thr806=) rs1488705625
NM_001077494.3(NFKB2):c.2601G>A (p.Ala867=) rs1438477157
NM_001077494.3(NFKB2):c.396-5C>T rs373971415

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