ClinVar Miner

List of variants reported as likely benign for Common variable immunodeficiency 2

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Total variants: 11
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HGVS dbSNP
NM_012452.2(TNFRSF13B):c.165C>T (p.Asn55=) rs756655390
NM_012452.2(TNFRSF13B):c.215G>A (p.Arg72His) rs55916807
NM_012452.2(TNFRSF13B):c.519C>T (p.Ala173=) rs151139237
NM_012452.2(TNFRSF13B):c.568G>C (p.Gly190Arg) rs150101848
NM_012452.2(TNFRSF13B):c.659T>C (p.Val220Ala) rs56063729
NM_012452.3(TNFRSF13B):c.105C>T (p.Pro35=) rs200868537
NM_012452.3(TNFRSF13B):c.226G>A (p.Gly76Ser) rs146436713
NM_012452.3(TNFRSF13B):c.561G>A (p.Lys187=) rs373469090
NM_012452.3(TNFRSF13B):c.593G>A (p.Arg198His) rs150974807
NM_012452.3(TNFRSF13B):c.648C>T (p.Ala216=) rs777265646
NM_012452.3(TNFRSF13B):c.843T>C (p.Ile281=) rs1597656219

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