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

rs2244169

From SNPedia

Orientationplus
Stabilizedplus
Make rs2244169(A;A)
Make rs2244169(A;T)
Make rs2244169(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position57592329
is asnp
is mentioned by
dbSNPrs2244169
ebirs2244169
HLIrs2244169
Exacrs2244169
Varsomers2244169
Maprs2244169
PheGenIrs2244169
hapmaprs2244169
1000 genomesrs2244169
hgdprs2244169
ensemblrs2244169
gopubmedrs2244169
geneviewrs2244169
scholarrs2244169
googlers2244169
pharmgkbrs2244169
gwascentralrs2244169
openSNPrs2244169
23andMers2244169
23andMe allrs2244169
SNP Nexus

SNPshotrs2244169
SNPdbers2244169
MSV3drs2244169
GWAS Ctlgrs2244169
GMAF0.3669
Max Magnitude
? (A;A) (A;T) (T;T) 28
[PMID 19169411OA-icon.png] Common variation in the SERPING1 gene is not associated with age-related macular degeneration in two independent groups of subjects.


[PMID 20062564OA-icon.png] An association study of SERPING1 gene and age-related macular degeneration in a Han Chinese population.


GET Evidence
rs2244169
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.476562
summary