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rs4308625

From SNPedia

Orientationplus
Stabilizedplus
Make rs4308625(C;C)
Make rs4308625(C;T)
Make rs4308625(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position14003077
is asnp
is mentioned by
dbSNPrs4308625
ebirs4308625
HLIrs4308625
Exacrs4308625
Varsomers4308625
Maprs4308625
PheGenIrs4308625
hapmaprs4308625
1000 genomesrs4308625
hgdprs4308625
ensemblrs4308625
gopubmedrs4308625
geneviewrs4308625
scholarrs4308625
googlers4308625
pharmgkbrs4308625
gwascentralrs4308625
openSNPrs4308625
23andMers4308625
23andMe allrs4308625
SNP Nexus

SNPshotrs4308625
SNPdbers4308625
MSV3drs4308625
GWAS Ctlgrs4308625
GMAF0.287
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 21239413] Association of IL2RA polymorphisms with susceptibility to multiple sclerosis is not explained by missense mutations in IL2RA