Variant (rsID / SNP)

rs11886868

rs11886868 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BCL11A. Location: chromosome 2, position 60,720,246. Clinical significance in the table: Benign.

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Reference-table entries

BCL11ABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:60720246
Cytoband: 2p16.1
HGVS: NM_022893.4(BCL11A):c.386-24278G>A
Allele change: Silent

Associated conditions / phenotypes

Fetal hemoglobin quantitative trait locus 5|Dias-Logan syndrome

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.