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rs4929984

From SNPedia

Orientationplus
Stabilizedplus
Make rs4929984(A;A)
Make rs4929984(A;C)
Make rs4929984(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position2003453
is asnp
is mentioned by
dbSNPrs4929984
ebirs4929984
HLIrs4929984
Exacrs4929984
Varsomers4929984
Maprs4929984
PheGenIrs4929984
hapmaprs4929984
1000 genomesrs4929984
hgdprs4929984
ensemblrs4929984
gopubmedrs4929984
geneviewrs4929984
scholarrs4929984
googlers4929984
pharmgkbrs4929984
gwascentralrs4929984
openSNPrs4929984
23andMers4929984
23andMe allrs4929984
SNP Nexus

SNPshotrs4929984
SNPdbers4929984
MSV3drs4929984
GWAS Ctlgrs4929984
GMAF0.4123
Max Magnitude
? (A;A) (A;C) (C;C) 28
[PMID 20639793OA-icon.png] Association of birth weight with polymorphisms in the IGF2, H19, and IGF2R genes


[PMID 16839189OA-icon.png] Human imprinted chromosomal regions are historical hot-spots of recombination.