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rs10733612

From SNPedia

Orientationplus
Stabilizedplus
Make rs10733612(C;C)
Make rs10733612(C;T)
Make rs10733612(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position114760770
is asnp
is mentioned by
dbSNPrs10733612
ebirs10733612
HLIrs10733612
Exacrs10733612
Varsomers10733612
Maprs10733612
PheGenIrs10733612
hapmaprs10733612
1000 genomesrs10733612
hgdprs10733612
ensemblrs10733612
gopubmedrs10733612
geneviewrs10733612
scholarrs10733612
googlers10733612
pharmgkbrs10733612
gwascentralrs10733612
openSNPrs10733612
23andMers10733612
23andMe allrs10733612
SNP Nexus

SNPshotrs10733612
SNPdbers10733612
MSV3drs10733612
GWAS Ctlgrs10733612
GMAF0.2084
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 19543369OA-icon.png] Comprehensive linkage and association analyses identify haplotype, near to the TNFSF15 gene, significantly associated with spondyloarthritis