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rs3910901

From SNPedia

Merged intors2590281
Orientationminus
Stabilizedminus
Make rs3910901(C;C)
Make rs3910901(C;G)
Make rs3910901(G;G)
ReferenceGRCh38 38.1/142
Chromosome12
is asnp
is mentioned by
dbSNPrs3910901
ebirs3910901
HLIrs3910901
Exacrs3910901
Varsomers3910901
Maprs3910901
PheGenIrs3910901
hapmaprs3910901
1000 genomesrs3910901
hgdprs3910901
ensemblrs3910901
gopubmedrs3910901
geneviewrs3910901
scholarrs3910901
googlers3910901
pharmgkbrs3910901
gwascentralrs3910901
openSNPrs3910901
23andMers3910901
23andMe allrs3910901
SNP Nexus

SNPshotrs3910901
SNPdbers3910901
MSV3drs3910901
GWAS Ctlgrs3910901
StatusMerged into rs2590281
Max Magnitude

[PMID 25648666] Polymorphisms of EHF-ELF5 genomic region and its association with pediatric asthma in the Taiwanese population