Have questions? Visit https://www.reddit.com/r/SNPedia

rs4252548

From SNPedia

Orientationminus
Stabilizedminus
Make rs4252548(A;A)
Make rs4252548(A;G)
Make rs4252548(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome19
Position55368304
GeneIL11
is asnp
is mentioned by
dbSNPrs4252548
dbSNP (classic)rs4252548
ClinGenrs4252548
ebirs4252548
HLIrs4252548
Exacrs4252548
Gnomadrs4252548
Varsomers4252548
LitVarrs4252548
Maprs4252548
PheGenIrs4252548
Biobankrs4252548
1000 genomesrs4252548
hgdprs4252548
ensemblrs4252548
geneviewrs4252548
scholarrs4252548
googlers4252548
pharmgkbrs4252548
gwascentralrs4252548
openSNPrs4252548
23andMers4252548
23andMe allrs4252548
SNPshotrs4252548
SNPdbers4252548
MSV3drs4252548
GWAS Ctlgrs4252548
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 28146470OA-icon.png] Rare and low-frequency coding variants alter human adult height.