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rs4072796

From SNPedia

Orientationplus
Stabilizedplus
Make rs4072796(C;C)
Make rs4072796(C;G)
Make rs4072796(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome12
Position7396400
GeneCD163L1
is asnp
is mentioned by
dbSNPrs4072796
dbSNP (classic)rs4072796
ClinGenrs4072796
ebirs4072796
HLIrs4072796
Exacrs4072796
Gnomadrs4072796
Varsomers4072796
LitVarrs4072796
Maprs4072796
PheGenIrs4072796
Biobankrs4072796
1000 genomesrs4072796
hgdprs4072796
ensemblrs4072796
geneviewrs4072796
scholarrs4072796
googlers4072796
pharmgkbrs4072796
gwascentralrs4072796
openSNPrs4072796
23andMers4072796
23andMe allrs4072796
SNPshotrs4072796
SNPdbers4072796
MSV3drs4072796
GWAS Ctlgrs4072796
Max Magnitude0
? (C;C) (C;G) (G;G) 28


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