rs76546355(A;G)

Increased risk of Behçet's disease

Magnitude
5.5Very important
Repute
Bad
On SNPedia
rs76546355(A;G)
Gene
None listed

Other genotypes of rs76546355

  1. A;AMost notableBadincreased risk of Behçet's diseaseVery important · 5.5
  2. G;GGoodcommon in complete genomicsTypical · 0.0

All about rs76546355

Notes

From SNPedia

HLA-B*51 allele and the rs76546355 MHC SNP are independent genetic risk factors for Behçet's disease in Iranian, and that positivity for the rs76546355 risk allele, but not for B*51, does correlate with specific demographic characteristics or clinical manifestations in Behçet's disease patients

Source and license

Adapted from rs76546355(A;G) on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.

SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.