List of variants in gene LRBA reported as benign for not specified

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: 34

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HGVS	dbSNP	gnomAD frequency
NM_001364905.1(LRBA):c.1756-140G>A	rs1148648	0.95669
NM_001364905.1(LRBA):c.1360-40A>G	rs1201207	0.95627
NM_001364905.1(LRBA):c.6551+84A>G	rs7674989	0.87341
NM_001364905.1(LRBA):c.4569+9C>T	rs186080	0.83135
NM_001364905.1(LRBA):c.5646-71G>A	rs1993109	0.69833
NM_001364905.1(LRBA):c.7849+10A>G	rs1813134	0.62993
NM_001364905.1(LRBA):c.7195-141T>C	rs13145548	0.61210
NM_001364905.1(LRBA):c.6921+60C>G	rs2292122	0.21963
NM_001364905.1(LRBA):c.6922-40C>A	rs2271043	0.21960
NM_001364905.1(LRBA):c.8077G>A (p.Ala2693Thr)	rs3749574	0.21105
NM_001364905.1(LRBA):c.8393C>T (p.Ser2798Leu)	rs2290846	0.18590
NM_001364905.1(LRBA):c.7630+31G>A	rs11737450	0.17416
NM_001364905.1(LRBA):c.5550T>C (p.Val1850=)	rs1129998	0.17226
NM_001364905.1(LRBA):c.3269C>G (p.Ala1090Gly)	rs1782360	0.12249
NM_001364905.1(LRBA):c.1347A>G (p.Ala449=)	rs1201208	0.10667
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.3874G>A (p.Val1292Ile)	rs34678304	0.00820
NM_001364905.1(LRBA):c.5100G>T (p.Leu1700=)	rs61741557	0.00815
NM_001364905.1(LRBA):c.1513A>G (p.Ile505Val)	rs35612775	0.00642
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.3568A>G (p.Met1190Val)	rs138173151	0.00282
NM_001364905.1(LRBA):c.2444A>G (p.Asn815Ser)	rs140666848	0.00218
NM_001364905.1(LRBA):c.*9G>T	rs150102345	0.00194
NM_001364905.1(LRBA):c.1015-10del	rs753223643
NM_001364905.1(LRBA):c.1015-20dup	rs753223643
NM_001364905.1(LRBA):c.217-10del	rs766044503
NM_001364905.1(LRBA):c.217-21dup	rs766044503
NM_001364905.1(LRBA):c.8469-487A>C
NM_001364905.1(LRBA):c.8469-707_8469-705dup

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