Variant (rsID / SNP)

rs11088969

rs11088969 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ITGB2. Location: chromosome 21, position 46,330,674. Clinical significance in the table: Benign.

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Reference-table entries

ITGB2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 21:46330674
Cytoband: 21q22.3
HGVS: NM_000211.5(ITGB2):c.24G>T (p.Leu8=)
Allele change: Synonymous_L8L

Associated conditions / phenotypes

Leukocyte adhesion deficiency 1

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.