rs3767155
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3767155(A;A) |
| Make rs3767155(A;G) |
| Make rs3767155(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 21558702 |
| Gene | ALPL |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3767155 |
| dbSNP (classic) | rs3767155 |
| ClinGen | rs3767155 |
| ebi | rs3767155 |
| HLI | rs3767155 |
| Exac | rs3767155 |
| Gnomad | rs3767155 |
| Varsome | rs3767155 |
| LitVar | rs3767155 |
| Map | rs3767155 |
| PheGenI | rs3767155 |
| Biobank | rs3767155 |
| 1000 genomes | rs3767155 |
| hgdp | rs3767155 |
| ensembl | rs3767155 |
| geneview | rs3767155 |
| scholar | rs3767155 |
| rs3767155 | |
| pharmgkb | rs3767155 |
| gwascentral | rs3767155 |
| openSNP | rs3767155 |
| 23andMe | rs3767155 |
| SNPshot | rs3767155 |
| SNPdbe | rs3767155 |
| MSV3d | rs3767155 |
| GWAS Ctlg | rs3767155 |
| GMAF | 0.2934 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
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| ||
[PMID 17195227] A study of 201 Canadian ankylosing spondylitis families concluded the ALPL (TNAP) haplotype G-G-T for SNPs rs3767155-rs3738099-rs1780329, respectively, is significantly associated with the disease but only in men.
[PMID 18769922] A study of 353 Chinese ankylosing spondylitis patients found no significant difference in allele, genotype or haplotype frequencies for this SNP in either case-control or family-based association studies, which indicated that the TNAP (also known as ALPL) gene is unlikely to play a major role in the susceptibility to ankylosing spondylitis in the Chinese Han population.
