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Variant (rsID / SNP)

rs45511401

ABCC1

rs45511401 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCC1. Location: chromosome 16, position 16,173,232. The table records no clinical significance for this variant.

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Reference-table entries

ABCC1Not classified
Variant type
missense_variant
Chromosome / position
16:16173232
HGVS
NM_004996.4,c.2012G>T,p.Gly671Val
Allele change
Missense_G671V

Associated conditions / phenotypes

Neutropenia|Neuroblastoma

Public references

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