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rs4982958

From SNPedia

Orientationplus
Stabilizedplus
Make rs4982958(C;C)
Make rs4982958(C;T)
Make rs4982958(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position24518659
is asnp
is mentioned by
dbSNPrs4982958
ebirs4982958
HLIrs4982958
Exacrs4982958
Varsomers4982958
Maprs4982958
PheGenIrs4982958
hapmaprs4982958
1000 genomesrs4982958
hgdprs4982958
ensemblrs4982958
gopubmedrs4982958
geneviewrs4982958
scholarrs4982958
googlers4982958
pharmgkbrs4982958
gwascentralrs4982958
openSNPrs4982958
23andMers4982958
23andMe allrs4982958
SNP Nexus

SNPshotrs4982958
SNPdbers4982958
MSV3drs4982958
GWAS Ctlgrs4982958
GMAF0.4325
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 22448455] Genetic variant rs4982958 at 14q11.2 is associated with allergic rhinitis in a Chinese Han population running title: 14q11.2 is a susceptibility locus for allergic rhinitis