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

rs11695685

From SNPedia

Orientationplus
Stabilizedplus
Make rs11695685(C;C)
Make rs11695685(C;T)
Make rs11695685(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position79695676
GeneCTNNA2
is asnp
is mentioned by
dbSNPrs11695685
ebirs11695685
HLIrs11695685
Exacrs11695685
Varsomers11695685
Maprs11695685
PheGenIrs11695685
hapmaprs11695685
1000 genomesrs11695685
hgdprs11695685
ensemblrs11695685
gopubmedrs11695685
geneviewrs11695685
scholarrs11695685
googlers11695685
pharmgkbrs11695685
gwascentralrs11695685
openSNPrs11695685
23andMers11695685
23andMe allrs11695685
SNP Nexus

SNPshotrs11695685
SNPdbers11695685
MSV3drs11695685
GWAS Ctlgrs11695685
GMAF0.2883
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18464913OA-icon.png]
Trait Protein quantitative trait loci
Title A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)
Risk Allele
P-val 4.9999999999999998E-7
Odds Ratio NR NR

[PMID 18464913OA-icon.png] Interleukin 10 (IL10) protein levels


GET Evidence
rs11695685
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.289062
summary