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rs1042229

From SNPedia

Orientationminus
Stabilizedminus
Make rs1042229(G;G)
Make rs1042229(G;T)
Make rs1042229(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position51746419
GeneFPR1
is asnp
is mentioned by
dbSNPrs1042229
ebirs1042229
HLIrs1042229
Exacrs1042229
Varsomers1042229
Maprs1042229
PheGenIrs1042229
hapmaprs1042229
1000 genomesrs1042229
hgdprs1042229
ensemblrs1042229
gopubmedrs1042229
geneviewrs1042229
scholarrs1042229
googlers1042229
pharmgkbrs1042229
gwascentralrs1042229
openSNPrs1042229
23andMers1042229
23andMe allrs1042229
SNP Nexus

SNPshotrs1042229
SNPdbers1042229
MSV3drs1042229
GWAS Ctlgrs1042229
GMAF0.4022
Max Magnitude
? (G;G) (G;T) (T;T) 28

[PMID 21216225] Polymorphisms of the formylpeptide receptor gene (FPR1) and susceptibility to stomach cancer in 1,531 consecutive autopsy cases


GET Evidence
FPR1-N192K
aa_change Asn192Lys
aa_change_short N192K
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.433631
summary



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