List of variants in gene LRBA reported as uncertain significance 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001364905.1(LRBA):c.3350G>T (p.Gly1117Val)	rs35977354	0.00462
NM_001364905.1(LRBA):c.5030A>G (p.Asn1677Ser)	rs17027133	0.00349
NM_001364905.1(LRBA):c.6448+17A>G	rs183652080	0.00274
NM_001364905.1(LRBA):c.1399A>G (p.Met467Val)	rs116355217	0.00225
NM_001364905.1(LRBA):c.3751A>G (p.Thr1251Ala)	rs143973442	0.00034
NM_001364905.1(LRBA):c.3262G>C (p.Glu1088Gln)	rs142075710	0.00023
NM_001364905.1(LRBA):c.3914G>A (p.Arg1305His)	rs144754728	0.00019
NM_001364905.1(LRBA):c.1316A>G (p.Asn439Ser)	rs572309256	0.00003
NM_001364905.1(LRBA):c.7865T>C (p.Val2622Ala)	rs541116943	0.00001

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