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rs9999118

From SNPedia

Orientationplus
Stabilizedplus
Make rs9999118(A;A)
Make rs9999118(A;G)
Make rs9999118(G;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position123130312
GeneSPATA5
is asnp
is mentioned by
dbSNPrs9999118
ebirs9999118
HLIrs9999118
Exacrs9999118
Varsomers9999118
Maprs9999118
PheGenIrs9999118
hapmaprs9999118
1000 genomesrs9999118
hgdprs9999118
ensemblrs9999118
gopubmedrs9999118
geneviewrs9999118
scholarrs9999118
googlers9999118
pharmgkbrs9999118
gwascentralrs9999118
openSNPrs9999118
23andMers9999118
23andMe allrs9999118
SNP Nexus

SNPshotrs9999118
SNPdbers9999118
MSV3drs9999118
GWAS Ctlgrs9999118
Max Magnitude
GWAS snp
PMID [PMID 24797007]
Trait Irritable bowel syndrome
Title Genome-wide association study identifies two novel genomic regions in irritable bowel syndrome.
Risk Allele G
P-val 8E-8
Odds Ratio 7.30 [3.53-15.03]