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rs1736135

From SNPedia

Orientationplus
Stabilizedplus
Make rs1736135(C;C)
Make rs1736135(C;T)
Make rs1736135(T;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position15432901
is asnp
is mentioned by
dbSNPrs1736135
ebirs1736135
HLIrs1736135
Exacrs1736135
Varsomers1736135
Maprs1736135
PheGenIrs1736135
hapmaprs1736135
1000 genomesrs1736135
hgdprs1736135
ensemblrs1736135
gopubmedrs1736135
geneviewrs1736135
scholarrs1736135
googlers1736135
pharmgkbrs1736135
gwascentralrs1736135
openSNPrs1736135
23andMers1736135
23andMe allrs1736135
SNP Nexus

SNPshotrs1736135
SNPdbers1736135
MSV3drs1736135
GWAS Ctlgrs1736135
GMAF0.2718
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 T
P-val 6.9999999999999998E-9
Odds Ratio 1.18 [NR]
GWAS snp
PMID [PMID 20228799OA-icon.png]
Trait Ulcerative colitis
Title Genome-wide association identifies multiple ulcerative colitis susceptibility loci
Risk Allele T
P-val 2E-7
Odds Ratio 1.20 [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
rs1736135
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.28125
summary