Variant (rsID / SNP)

rs2229109

rs2229109 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCB1. Location: chromosome 7, position 87,179,809. Clinical significance in the table: Benign.

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Reference-table entries

ABCB1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 7:87179809
Cytoband: 7q21.12
HGVS: NM_001348946.2(ABCB1):c.1199G>A (p.Ser400Asn)
Allele change: Missense_S400I

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.