ClinVar Miner

List of variants in gene LRBA 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: 19
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HGVS dbSNP
NM_001199282.2(LRBA):c.3948A>G (p.Gln1316=) rs35154927
NM_006726.4(LRBA):c.1014+7A>C rs375965457
NM_006726.4(LRBA):c.1015-8T>C rs762827813
NM_006726.4(LRBA):c.1296T>C (p.Leu432=) rs111753976
NM_006726.4(LRBA):c.1713C>T (p.His571=) rs145812385
NM_006726.4(LRBA):c.2064T>C (p.His688=) rs145198687
NM_006726.4(LRBA):c.3373C>T (p.Leu1125=) rs138238756
NM_006726.4(LRBA):c.4323G>A (p.Arg1441=) rs145003932
NM_006726.4(LRBA):c.5004G>A (p.Pro1668=) rs775567440
NM_006726.4(LRBA):c.5460T>G (p.Pro1820=) rs565770808
NM_006726.4(LRBA):c.6196G>A (p.Val2066Met) rs138428438
NM_006726.4(LRBA):c.6354C>T (p.Ile2118=) rs199753191
NM_006726.4(LRBA):c.7011T>C (p.Asp2337=) rs1172980980
NM_006726.4(LRBA):c.7131T>C (p.Tyr2377=) rs751952359
NM_006726.4(LRBA):c.7602C>T (p.Pro2534=) rs1372828165
NM_006726.4(LRBA):c.7911T>C (p.His2637=) rs946590569
NM_006726.4(LRBA):c.8046A>C (p.Pro2682=) rs1553994424
NM_006726.4(LRBA):c.8082C>T (p.Thr2694=) rs144225937
NM_006726.4(LRBA):c.950G>A (p.Arg317Gln) rs151021623

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