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rs10486483

From SNPedia

Orientationplus
Stabilizedplus
Make rs10486483(A;A)
Make rs10486483(A;G)
Make rs10486483(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position26852821
GeneSKAP2
is asnp
is mentioned by
dbSNPrs10486483
ebirs10486483
HLIrs10486483
Exacrs10486483
Varsomers10486483
Maprs10486483
PheGenIrs10486483
hapmaprs10486483
1000 genomesrs10486483
hgdprs10486483
ensemblrs10486483
gopubmedrs10486483
geneviewrs10486483
scholarrs10486483
googlers10486483
pharmgkbrs10486483
gwascentralrs10486483
openSNPrs10486483
23andMers10486483
23andMe allrs10486483
SNP Nexus

SNPshotrs10486483
SNPdbers10486483
MSV3drs10486483
GWAS Ctlgrs10486483
GMAF0.1708
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23128233OA-icon.png]
Trait Crohn's disease
Title Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
Risk Allele A
P-val 3E-8
Odds Ratio 1.09 [1.048-1.13]