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rs2509897

From SNPedia

Orientationminus
Stabilizedminus
Make rs2509897(C;C)
Make rs2509897(C;G)
Make rs2509897(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position57595144
is asnp
is mentioned by
dbSNPrs2509897
ebirs2509897
HLIrs2509897
Exacrs2509897
Varsomers2509897
Maprs2509897
PheGenIrs2509897
hapmaprs2509897
1000 genomesrs2509897
hgdprs2509897
ensemblrs2509897
gopubmedrs2509897
geneviewrs2509897
scholarrs2509897
googlers2509897
pharmgkbrs2509897
gwascentralrs2509897
openSNPrs2509897
23andMers2509897
23andMe allrs2509897
SNP Nexus

SNPshotrs2509897
SNPdbers2509897
MSV3drs2509897
GWAS Ctlgrs2509897
GMAF0.2222
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 20161815OA-icon.png] SERPING1 polymorphisms in polypoidal choroidal vasculopathy

[PMID 19169411OA-icon.png] Common variation in the SERPING1 gene is not associated with age-related macular degeneration in two independent groups of subjects.


GET Evidence
rs2509897
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.71875
summary