Rs10995271

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ReferenceGRCh37 37.1/131
Chromosome10
Position64438486
is asnp
is mentioned by
dbSNPrs10995271
PheGenIrs10995271
nextbiors10995271
hapmaprs10995271
1000 genomesrs10995271
hgdprs10995271
ensemblrs10995271
gopubmedrs10995271
geneviewrs10995271
scholarrs10995271
googlers10995271
pharmgkbrs10995271
gwascentralrs10995271
openSNPrs10995271
23andMers10995271
23andMe allrs10995271
SNP Nexus

SNPshotrs10995271
SNPdbers10995271
MSV3drs10995271
GMAF0.3627
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 18587394OA-icon.png]
Trait Crohn's disease
Title Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease
Risk Allele C
P-val 3.9999999999999998E-20
Odds Ratio 1.25 [NR]
OMIM612255
DescINFLAMMATORY BOWEL DISEASE 15; IBD15
Variant
Relatedalso
[PMID 19915572OA-icon.png] Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.


[PMID 21304977OA-icon.png] An investigation of genome-wide studies reported susceptibility loci for ulcerative colitis shows limited replication in north Indians.


GET Evidence
rs10995271
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.359375
summary



[PMID 24365559] Crohn's disease susceptibility variants in Colombian tuberculosis patients