Variants in gene LRBA with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 14

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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.7564A>C (p.Thr2522Pro)	rs62346982	0.00470
NM_001364905.1(LRBA):c.3826-5A>G	rs114629781	0.00462
NM_001364905.1(LRBA):c.2526T>C (p.Phe842=)	rs139428189	0.00376
NM_001364905.1(LRBA):c.5030A>G (p.Asn1677Ser)	rs17027133	0.00349
NM_001364905.1(LRBA):c.2444A>G (p.Asn815Ser)	rs140666848	0.00218
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.2275A>C (p.Met759Leu)	rs191118242	0.00022
NM_001364905.1(LRBA):c.2067+11A>G	rs185860143	0.00019
NM_001364905.1(LRBA):c.3423C>T (p.Ala1141=)	rs141442145	0.00015
NM_001364905.1(LRBA):c.1015-20dup	rs753223643

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