rs13202464
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common/normal |
(A;G) | 3 | likely to be a carrier of one HLA-B27 allele, possible risk for B27 Syndromes. |
(G;G) | 3 | likely to carry two HLA-B27 alleles, possible risk for B27 Syndromes. |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31376806 |
Gene | FGFR3P1 |
is a | snp |
is | mentioned by |
dbSNP | rs13202464 |
dbSNP (classic) | rs13202464 |
ClinGen | rs13202464 |
ebi | rs13202464 |
HLI | rs13202464 |
Exac | rs13202464 |
Gnomad | rs13202464 |
Varsome | rs13202464 |
LitVar | rs13202464 |
Map | rs13202464 |
PheGenI | rs13202464 |
Biobank | rs13202464 |
1000 genomes | rs13202464 |
hgdp | rs13202464 |
ensembl | rs13202464 |
geneview | rs13202464 |
scholar | rs13202464 |
rs13202464 | |
pharmgkb | rs13202464 |
gwascentral | rs13202464 |
openSNP | rs13202464 |
23andMe | rs13202464 |
SNPshot | rs13202464 |
SNPdbe | rs13202464 |
MSV3d | rs13202464 |
GWAS Ctlg | rs13202464 |
GMAF | 0.06152 |
Max Magnitude | 3 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
See: HLA-B27 Syndromes.
Not all alleles of HLA-B27 are at risk for B27 Syndromes, please check the HLA-B27 page for details.
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