Variant (rsID / SNP)
rs11735845
rs11735845 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRBA. Location: chromosome 4, position 151,765,336. Clinical significance in the table: Benign.
Reference-table entries
LRBABenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 4:151765336
- Cytoband
- 4q31.3
- HGVS
- NM_001364905.1(LRBA):c.4485C>T (p.Gly1495=)
- Allele change
- Synonymous_G1495G
Associated conditions / phenotypes
Combined immunodeficiency due to LRBA deficiency
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.