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rs2099884

From SNPedia

Orientationminus
Stabilizedminus
Make rs2099884(C;C)
Make rs2099884(C;T)
Make rs2099884(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position141842417
is asnp
is mentioned by
dbSNPrs2099884
ebirs2099884
HLIrs2099884
Exacrs2099884
Varsomers2099884
Maprs2099884
PheGenIrs2099884
hapmaprs2099884
1000 genomesrs2099884
hgdprs2099884
ensemblrs2099884
gopubmedrs2099884
geneviewrs2099884
scholarrs2099884
googlers2099884
pharmgkbrs2099884
gwascentralrs2099884
openSNPrs2099884
23andMers2099884
23andMe allrs2099884
SNP Nexus

SNPshotrs2099884
SNPdbers2099884
MSV3drs2099884
GWAS Ctlgrs2099884
GMAF0.2447
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 24348519OA-icon.png] EMR-linked GWAS study: investigation of variation landscape of loci for body mass index in children