Variant (rsID / SNP)

rs1801274

rs1801274 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FCGR2A. Location: chromosome 1, position 161,479,745. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

FCGR2ABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:161479745
Cytoband: 1q23.3
HGVS: NM_001136219.3(FCGR2A):c.500A>G (p.His167Arg)
Allele change: Missense_H167R

Associated conditions / phenotypes

Lupus nephritis, susceptibility to|Pseudomonas aeruginosa, susceptibility to chronic infection by, in cystic fibrosis|Malaria, severe, 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.