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rs3738099

From SNPedia

Merged intors3200254
Orientationplus
Stabilizedplus
Make rs3738099(C;C)
Make rs3738099(C;T)
Make rs3738099(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position21568242
GeneALPL
is asnp
is mentioned by
dbSNPrs3738099
ebirs3738099
HLIrs3738099
Exacrs3738099
Varsomers3738099
Maprs3738099
PheGenIrs3738099
hapmaprs3738099
1000 genomesrs3738099
hgdprs3738099
ensemblrs3738099
gopubmedrs3738099
geneviewrs3738099
scholarrs3738099
googlers3738099
pharmgkbrs3738099
gwascentralrs3738099
openSNPrs3738099
23andMers3738099
23andMe allrs3738099
SNP Nexus

SNPshotrs3738099
SNPdbers3738099
MSV3drs3738099
GWAS Ctlgrs3738099
StatusMerged into rs3200254
Max Magnitude
? (C;C) (C;T) (T;T) 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.