Variant (rsID / SNP)

rs2229038

rs2229038 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BCR. Location: chromosome 22, position 23,634,790. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

BCRBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 22:23634790
Cytoband: 22q11.23
HGVS: NM_004327.4(BCR):c.2845G>A (p.Val949Ile)
Allele change: Missense_V949I

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.