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rs7979673

From SNPedia

Orientationplus
Stabilizedplus
Make rs7979673(C;C)
Make rs7979673(C;T)
Make rs7979673(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position65833477
GeneHMGA2
is asnp
is mentioned by
dbSNPrs7979673
dbSNP (classic)rs7979673
ClinGenrs7979673
ebirs7979673
HLIrs7979673
Exacrs7979673
Gnomadrs7979673
Varsomers7979673
LitVarrs7979673
Maprs7979673
PheGenIrs7979673
Biobankrs7979673
1000 genomesrs7979673
hgdprs7979673
ensemblrs7979673
geneviewrs7979673
scholarrs7979673
googlers7979673
pharmgkbrs7979673
gwascentralrs7979673
openSNPrs7979673
23andMers7979673
SNPshotrs7979673
SNPdbers7979673
MSV3drs7979673
GWAS Ctlgrs7979673
GMAF0.1428
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 21998595OA-icon.png]
Trait
Title Identification, replication, and fine-mapping of Loci associated with adult height in individuals of african ancestry.
Risk Allele T
P-val 7E-10
Odds Ratio 0.0580 None