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rs3767155

From SNPedia

Orientationminus
Stabilizedminus
Make rs3767155(A;A)
Make rs3767155(A;G)
Make rs3767155(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position21558702
GeneALPL
is asnp
is mentioned by
dbSNPrs3767155
ebirs3767155
HLIrs3767155
Exacrs3767155
Varsomers3767155
Maprs3767155
PheGenIrs3767155
hapmaprs3767155
1000 genomesrs3767155
hgdprs3767155
ensemblrs3767155
gopubmedrs3767155
geneviewrs3767155
scholarrs3767155
googlers3767155
pharmgkbrs3767155
gwascentralrs3767155
openSNPrs3767155
23andMers3767155
23andMe allrs3767155
SNP Nexus

SNPshotrs3767155
SNPdbers3767155
MSV3drs3767155
GWAS Ctlgrs3767155
GMAF0.2934
Max Magnitude
? (A;A) (A;G) (G;G) 28
[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.