Variant (rsID / SNP)

rs2229067

rs2229067 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABL1. Location: chromosome 9, position 133,760,592. Clinical significance in the table: Benign.

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Reference-table entries

ABL1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 9:133760592
Cytoband: 9q34.12
HGVS: NM_005157.6(ABL1):c.2915C>T (p.Ser972Leu)
Allele change: Missense_S991L

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.