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rs5030878

From SNPedia

Orientationminus
Stabilizedminus
Make rs5030878(C;C)
Make rs5030878(C;T)
Make rs5030878(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position51746963
GeneFPR1, LOC100287831
is asnp
is mentioned by
dbSNPrs5030878
ebirs5030878
HLIrs5030878
Exacrs5030878
Varsomers5030878
Maprs5030878
PheGenIrs5030878
hapmaprs5030878
1000 genomesrs5030878
hgdprs5030878
ensemblrs5030878
gopubmedrs5030878
geneviewrs5030878
scholarrs5030878
googlers5030878
pharmgkbrs5030878
gwascentralrs5030878
openSNPrs5030878
23andMers5030878
23andMe allrs5030878
SNP Nexus

SNPshotrs5030878
SNPdbers5030878
MSV3drs5030878
GWAS Ctlgrs5030878
GMAF0.1736
Max Magnitude
? (C;C) (C;T) (T;T) 28



[PMID 21144844] Human formyl peptide receptor 1 C32T SNP interacts with age and is associated with blood pressure levels.


GET Evidence
FPR1-I11T
aa_change Ile11Thr
aa_change_short I11T
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.773099
summary



[PMID 23373827OA-icon.png] V101L of human formyl peptide receptor 1 (FPR1) increases receptor affinity and augments the antagonism mediated by cyclosporins.