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: 56
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HGVS dbSNP
NM_001364905.1(LRBA):c.1014+7A>C rs375965457
NM_001364905.1(LRBA):c.103C>T (p.Leu35=)
NM_001364905.1(LRBA):c.1071C>T (p.Phe357=)
NM_001364905.1(LRBA):c.1219T>C (p.Leu407=)
NM_001364905.1(LRBA):c.1551A>G (p.Glu517=)
NM_001364905.1(LRBA):c.1695C>T (p.Leu565=)
NM_001364905.1(LRBA):c.1713C>T (p.His571=) rs145812385
NM_001364905.1(LRBA):c.1755+10A>G
NM_001364905.1(LRBA):c.2064T>C (p.His688=) rs145198687
NM_001364905.1(LRBA):c.2406A>G (p.Lys802=)
NM_001364905.1(LRBA):c.2466T>G (p.Ile822Met)
NM_001364905.1(LRBA):c.2619C>G (p.Leu873=)
NM_001364905.1(LRBA):c.2811G>A (p.Arg937=) rs367738505
NM_001364905.1(LRBA):c.3009T>A (p.Ser1003=)
NM_001364905.1(LRBA):c.3012A>G (p.Ala1004=)
NM_001364905.1(LRBA):c.3207C>A (p.Gly1069=) rs762031957
NM_001364905.1(LRBA):c.3373C>T (p.Leu1125=) rs138238756
NM_001364905.1(LRBA):c.3726G>A (p.Ala1242=)
NM_001364905.1(LRBA):c.375T>A (p.Leu125=)
NM_001364905.1(LRBA):c.3948A>G (p.Gln1316=) rs35154927
NM_001364905.1(LRBA):c.4100A>G (p.Asn1367Ser)
NM_001364905.1(LRBA):c.4323G>A (p.Arg1441=) rs145003932
NM_001364905.1(LRBA):c.4338A>G (p.Leu1446=) rs201059532
NM_001364905.1(LRBA):c.4377A>G (p.Gln1459=)
NM_001364905.1(LRBA):c.4416G>A (p.Leu1472=)
NM_001364905.1(LRBA):c.4515G>A (p.Arg1505=)
NM_001364905.1(LRBA):c.4591T>G (p.Phe1531Val) rs114610541
NM_001364905.1(LRBA):c.4956G>A (p.Pro1652=)
NM_001364905.1(LRBA):c.5004G>A (p.Pro1668=) rs775567440
NM_001364905.1(LRBA):c.5460T>G (p.Pro1820=) rs565770808
NM_001364905.1(LRBA):c.6036C>T (p.Ala2012=)
NM_001364905.1(LRBA):c.6163G>A (p.Val2055Met) rs138428438
NM_001364905.1(LRBA):c.6321C>T (p.Ile2107=) rs199753191
NM_001364905.1(LRBA):c.6322G>A (p.Asp2108Asn) rs142598024
NM_001364905.1(LRBA):c.6331-8C>G
NM_001364905.1(LRBA):c.6375A>G (p.Thr2125=)
NM_001364905.1(LRBA):c.6396T>C (p.Ser2132=)
NM_001364905.1(LRBA):c.6662T>C (p.Ile2221Thr) rs116526975
NM_001364905.1(LRBA):c.6780+8C>T
NM_001364905.1(LRBA):c.6887C>A (p.Thr2296Asn) rs151286835
NM_001364905.1(LRBA):c.6906A>G (p.Ala2302=)
NM_001364905.1(LRBA):c.6978T>C (p.Asp2326=) rs1172980980
NM_001364905.1(LRBA):c.6979C>A (p.Arg2327=)
NM_001364905.1(LRBA):c.7098T>C (p.Tyr2366=) rs751952359
NM_001364905.1(LRBA):c.7569C>T (p.Pro2523=) rs1372828165
NM_001364905.1(LRBA):c.7605G>A (p.Ala2535=)
NM_001364905.1(LRBA):c.7878T>C (p.His2626=) rs946590569
NM_001364905.1(LRBA):c.787C>G (p.Leu263Val) rs143625481
NM_001364905.1(LRBA):c.7887C>T (p.Val2629=)
NM_001364905.1(LRBA):c.8013A>C (p.Pro2671=) rs1553994424
NM_001364905.1(LRBA):c.8049C>T (p.Thr2683=) rs144225937
NM_001364905.1(LRBA):c.8061T>C (p.Tyr2687=)
NM_001364905.1(LRBA):c.8133C>T (p.Leu2711=)
NM_001364905.1(LRBA):c.8200C>T (p.Leu2734Phe)
NM_001364905.1(LRBA):c.8517C>T (p.Asn2839=)
NM_001364905.1(LRBA):c.950G>A (p.Arg317Gln) rs151021623

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