List of variants in gene LRBA reported as likely benign for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 36

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001364905.1(LRBA):c.5989C>T (p.Arg1997Cys)	rs35879351	0.02129
NM_001364905.1(LRBA):c.2170A>G (p.Ile724Val)	rs72719663	0.01896
NM_001364905.1(LRBA):c.5171+20G>A	rs116225517	0.00791
NM_001364905.1(LRBA):c.3825+15T>G	rs74366731	0.00494
NM_001364905.1(LRBA):c.7564A>C (p.Thr2522Pro)	rs62346982	0.00470
NM_001364905.1(LRBA):c.2526T>C (p.Phe842=)	rs139428189	0.00376
NM_001364905.1(LRBA):c.1399A>G (p.Met467Val)	rs116355217	0.00225
NM_001364905.1(LRBA):c.2444A>G (p.Asn815Ser)	rs140666848	0.00218
NM_001364905.1(LRBA):c.7404T>C (p.Ser2468=)	rs150550923	0.00185
NM_001364905.1(LRBA):c.2637G>A (p.Lys879=)	rs138956153	0.00170
NM_001364905.1(LRBA):c.8551C>T (p.Arg2851Cys)	rs145709687	0.00152
NM_001364905.1(LRBA):c.4591T>G (p.Phe1531Val)	rs114610541	0.00131
NM_001364905.1(LRBA):c.2340A>G (p.Thr780=)	rs79392371	0.00127
NM_001364905.1(LRBA):c.3948A>G (p.Gln1316=)	rs35154927	0.00125
NM_001364905.1(LRBA):c.1713C>T (p.His571=)	rs145812385	0.00101
NM_001364905.1(LRBA):c.5241T>C (p.Asn1747=)	rs72719631	0.00099
NM_001364905.1(LRBA):c.6387A>C (p.Ser2129=)	rs144748889	0.00096
NM_001364905.1(LRBA):c.3009T>A (p.Ser1003=)	rs149919062	0.00036
NM_001364905.1(LRBA):c.8061T>C (p.Tyr2687=)	rs146768056	0.00016
NM_001364905.1(LRBA):c.1071C>T (p.Phe357=)	rs749749471	0.00012
NM_001364905.1(LRBA):c.6375A>G (p.Thr2125=)	rs541432702	0.00005
NM_001364905.1(LRBA):c.6273C>T (p.Ser2091=)	rs146901365	0.00004
NM_001364905.1(LRBA):c.2586A>G (p.Gln862=)	rs763553802	0.00003
NM_001364905.1(LRBA):c.5502G>A (p.Leu1834=)	rs1002015795	0.00001
NM_001364905.1(LRBA):c.8200C>T (p.Leu2734Phe)	rs372949000	0.00001
NM_001364905.1(LRBA):c.1015-20dup	rs753223643
NM_001364905.1(LRBA):c.114G>T (p.Gly38=)	rs72721739
NM_001364905.1(LRBA):c.214C>T (p.Leu72=)	rs572995926
NM_001364905.1(LRBA):c.217-5G>T	rs74318720
NM_001364905.1(LRBA):c.2820A>G (p.Gln940=)
NM_001364905.1(LRBA):c.3264G>A (p.Glu1088=)
NM_001364905.1(LRBA):c.3373C>T (p.Leu1125=)	rs138238756
NM_001364905.1(LRBA):c.6046+1911A>G	rs1581776058
NM_001364905.1(LRBA):c.6424C>T (p.Leu2142=)	rs1438925105
NM_001364905.1(LRBA):c.8018-13dup	rs773155703
NM_001364905.1(LRBA):c.834A>G (p.Ser278=)	rs1329260934

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.