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rs3819299(C;C)

From SNPedia

likely to carry two HLA-B27 alleles, possible risk for B27 Syndromes.
Is agenotype
ofrs3819299
GeneHLA-B
Chromosome6
Position31,354,590
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(A;A) 0 common in clinvar
(A;C) 3 likely to carry one HLA-B27 allele, possible risk for B27 Syndromes.
(C;C) 3 likely to carry two HLA-B27 alleles, possible risk for B27 Syndromes.

See details at: HLA-B27 Syndromes.
Not all allelles of HLA-B27 are at risk for B27 Syndromes, please check the HLA-B27 page for details.