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rs10801047

From SNPedia

Orientationplus
Stabilizedplus
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ReferenceGRCh38 38.1/141
Chromosome1
Position191590226
is asnp
is mentioned by
dbSNPrs10801047
ebirs10801047
HLIrs10801047
Exacrs10801047
Varsomers10801047
Maprs10801047
PheGenIrs10801047
hapmaprs10801047
1000 genomesrs10801047
hgdprs10801047
ensemblrs10801047
gopubmedrs10801047
geneviewrs10801047
scholarrs10801047
googlers10801047
pharmgkbrs10801047
gwascentralrs10801047
openSNPrs10801047
23andMers10801047
23andMe allrs10801047
SNP Nexus

SNPshotrs10801047
SNPdbers10801047
MSV3drs10801047
GWAS Ctlgrs10801047
GMAF0.1878
Max Magnitude
? (A;A) (A;T) (T;T) 28
GWAS
SNP rs10801047
PubMedID [PMID 17554261OA-icon.png]
Condition Crohn's disease
Gene Intergenic
Risk Allele
pValue 3.00E-008
OR 1.47
95% CI 1.22-1.76



[PMID 18853133OA-icon.png] Gene variants influencing measures of inflammation or predisposing to autoimmune and inflammatory diseases are not associated with the risk of type 2 diabetes.

[PMID 19140132OA-icon.png] Unbiased estimation of odds ratios: combining genomewide association scans with replication studies.


GET Evidence
rs10801047
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.733333
summary