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rs17582416

From SNPedia

Orientationplus
Stabilizedplus
Make rs17582416(G;G)
Make rs17582416(G;T)
Make rs17582416(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position34998722
is asnp
is mentioned by
dbSNPrs17582416
ebirs17582416
HLIrs17582416
Exacrs17582416
Varsomers17582416
Maprs17582416
PheGenIrs17582416
hapmaprs17582416
1000 genomesrs17582416
hgdprs17582416
ensemblrs17582416
gopubmedrs17582416
geneviewrs17582416
scholarrs17582416
googlers17582416
pharmgkbrs17582416
gwascentralrs17582416
openSNPrs17582416
23andMers17582416
23andMe allrs17582416
SNP Nexus

SNPshotrs17582416
SNPdbers17582416
MSV3drs17582416
GWAS Ctlgrs17582416
GMAF0.315
Max Magnitude
? (G;G) (G;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 G
P-val 2.0000000000000001E-9
Odds Ratio 1.16 [NR]
OMIM266600
Desc
Variant
Relatedalso
[PMID 19068216OA-icon.png] Investigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationship.

[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
rs17582416
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.31746
summary