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Variant (rsID / SNP)

rs2271862

ABCA2

rs2271862 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCA2. Location: chromosome 9, position 139,906,359. The table records no clinical significance for this variant.

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Reference-table entries

ABCA2Not classified
Variant type
synonymous_variant
Chromosome / position
9:139906359
HGVS
NM_212533.3,c.5562C>T,p.His1854His
Allele change
Synonymous_H1854H

Associated conditions / phenotypes

Neutropenia

Public references

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