Variant (rsID / SNP)

rs4795895

rs4795895 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCL11. Location: chromosome 17, position 32,611,446. Clinical significance in the table: protective.

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Reference-table entries

CCL11Protective

Clinical significance (as recorded): protective
Variant type: single nucleotide variant
Chromosome / position: 17:32611446
Cytoband: 17q12
HGVS: NG_012212.1:g.3760=

Associated conditions / phenotypes

Susceptibility to HIV infection

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.