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rs76523431

From SNPedia

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Make rs76523431(A;A)
Make rs76523431(A;G)
Make rs76523431(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position40443555
is asnp
is mentioned by
dbSNPrs76523431
ebirs76523431
HLIrs76523431
Exacrs76523431
Varsomers76523431
Maprs76523431
PheGenIrs76523431
hapmaprs76523431
1000 genomesrs76523431
hgdprs76523431
ensemblrs76523431
gopubmedrs76523431
geneviewrs76523431
scholarrs76523431
googlers76523431
pharmgkbrs76523431
gwascentralrs76523431
openSNPrs76523431
23andMers76523431
23andMe allrs76523431
SNP Nexus

SNPshotrs76523431
SNPdbers76523431
MSV3drs76523431
GWAS Ctlgrs76523431
Max Magnitude

[PMID 26538147OA-icon.png] PTGER4 gene variant rs76523431 is a candidate risk factor for radiological joint damage in rheumatoid arthritis patients: a genetic study of six cohorts