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rs4648889

From SNPedia

Orientationplus
Stabilizedplus
Make rs4648889(A;A)
Make rs4648889(A;G)
Make rs4648889(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position24967338
is asnp
is mentioned by
dbSNPrs4648889
dbSNP (classic)rs4648889
ClinGenrs4648889
ebirs4648889
HLIrs4648889
Exacrs4648889
Gnomadrs4648889
Varsomers4648889
LitVarrs4648889
Maprs4648889
PheGenIrs4648889
Biobankrs4648889
1000 genomesrs4648889
hgdprs4648889
ensemblrs4648889
geneviewrs4648889
scholarrs4648889
googlers4648889
pharmgkbrs4648889
gwascentralrs4648889
openSNPrs4648889
23andMers4648889
SNPshotrs4648889
SNPdbers4648889
MSV3drs4648889
GWAS Ctlgrs4648889
Max Magnitude0

[PMID 26452539OA-icon.png] The genetic association of RUNX3 with ankylosing spondylitis can be explained by allele-specific effects on IRF4 recruitment that alter gene expression

[PMID 33284381] Replication study and meta-analysis indicate a suggestive association of RUNX3 locus with primary biliary cholangitis.