Have questions? Visit https://www.reddit.com/r/SNPedia

rs668853

From SNPedia

Orientationminus
Stabilizedplus
Make rs668853(A;A)
Make rs668853(A;G)
Make rs668853(G;G)
ReferenceGRCh38 38.1/142
Chromosome9
Position82696232
is asnp
is mentioned by
dbSNPrs668853
ebirs668853
HLIrs668853
Exacrs668853
Varsomers668853
Maprs668853
PheGenIrs668853
hapmaprs668853
1000 genomesrs668853
hgdprs668853
ensemblrs668853
gopubmedrs668853
geneviewrs668853
scholarrs668853
googlers668853
pharmgkbrs668853
gwascentralrs668853
openSNPrs668853
23andMers668853
23andMe allrs668853
SNP Nexus

SNPshotrs668853
SNPdbers668853
MSV3drs668853
GWAS Ctlgrs668853
GMAF0.4353
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19122664OA-icon.png]
Trait Ulcerative colitis
Title Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study
Risk Allele G
P-val 0.000002
Odds Ratio 1.20 None



[PMID 20823317OA-icon.png] is-rSNP: a novel technique for in silico regulatory SNP detection.


GET Evidence
rs668853
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.554688
summary