List of variants in gene LRBA reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001364905.1(LRBA):c.6781-3C>T	rs58873298	0.02593
NM_001364905.1(LRBA):c.2634T>G (p.Pro878=)	rs17027154	0.02479
NM_001364905.1(LRBA):c.7630+10G>C	rs57901153	0.02351
NM_001364905.1(LRBA):c.5989C>T (p.Arg1997Cys)	rs35879351	0.02129
NM_001364905.1(LRBA):c.4485C>T (p.Gly1495=)	rs11735845	0.02120
NM_001364905.1(LRBA):c.2170A>G (p.Ile724Val)	rs72719663	0.01896
NM_001364905.1(LRBA):c.3689G>A (p.Gly1230Asp)	rs34708681	0.00859
NM_001364905.1(LRBA):c.5100G>T (p.Leu1700=)	rs61741557	0.00815
NM_001364905.1(LRBA):c.5171+20G>A	rs116225517	0.00791
NM_001364905.1(LRBA):c.7564A>C (p.Thr2522Pro)	rs62346982	0.00470
NM_001364905.1(LRBA):c.2526T>C (p.Phe842=)	rs139428189	0.00376

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