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rs9877457

From SNPedia

Orientationplus
Stabilizedplus
Make rs9877457(A;A)
Make rs9877457(A;G)
Make rs9877457(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position135564539
is asnp
is mentioned by
dbSNPrs9877457
ebirs9877457
HLIrs9877457
Exacrs9877457
Varsomers9877457
Maprs9877457
PheGenIrs9877457
hapmaprs9877457
1000 genomesrs9877457
hgdprs9877457
ensemblrs9877457
gopubmedrs9877457
geneviewrs9877457
scholarrs9877457
googlers9877457
pharmgkbrs9877457
gwascentralrs9877457
openSNPrs9877457
23andMers9877457
23andMe allrs9877457
SNP Nexus

SNPshotrs9877457
SNPdbers9877457
MSV3drs9877457
GWAS Ctlgrs9877457
GMAF0.4803
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 21763378] Associations of EPHB1 polymorphisms with hepatocellular carcinoma in the Korean population