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Variant (rsID / SNP)

rs17822471

ABCC11

rs17822471 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCC11. Location: chromosome 16, position 48,242,379. The table records no clinical significance for this variant.

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Reference-table entries

ABCC11Not classified
Variant type
missense_variant
Chromosome / position
16:48242379
HGVS
NM_001370496.1,c.1637C>T,p.Thr546Met
Allele change
Missense_T546M

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.