Variant (rsID / SNP)

rs9264942

rs9264942 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HLA-C, LOC112267902. Location: chromosome 6, position 31,274,380. Clinical significance in the table: risk factor.

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Reference-table entries

HLA-CRisk factor

Clinical significance (as recorded): risk factor
Variant type: single nucleotide variant
Chromosome / position: 6:31274380
Cytoband: 6p21.33
HGVS: NC_000006.12:g.31306603T>C

Associated conditions / phenotypes

HIV-1 viremia, susceptibility to

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.