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rs2274910

From SNPedia

Orientationplus
Stabilizedplus
Make rs2274910(C;C)
Make rs2274910(C;T)
Make rs2274910(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position160882256
GeneITLN1
is asnp
is mentioned by
dbSNPrs2274910
ebirs2274910
HLIrs2274910
Exacrs2274910
Varsomers2274910
Maprs2274910
PheGenIrs2274910
hapmaprs2274910
1000 genomesrs2274910
hgdprs2274910
ensemblrs2274910
gopubmedrs2274910
geneviewrs2274910
scholarrs2274910
googlers2274910
pharmgkbrs2274910
gwascentralrs2274910
openSNPrs2274910
23andMers2274910
23andMe allrs2274910
SNP Nexus

SNPshotrs2274910
SNPdbers2274910
MSV3drs2274910
GWAS Ctlgrs2274910
GMAF0.3976
Max Magnitude
? (C;C) (C;T) (T;T) 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 1.0000000000000001E-9
Odds Ratio 1.14 [NR]

[PMID 19068216OA-icon.png] Investigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationship.

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


GET Evidence
rs2274910
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.57534
summary



[PMID 22573572] Phenotype-genotype profiles in Crohn's disease predicted by genetic markers in autophagy-related genes (GOIA study II).