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rs7968682

From SNPedia

Orientationplus
Stabilizedplus
Make rs7968682(G;G)
Make rs7968682(G;T)
Make rs7968682(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position65978100
is asnp
is mentioned by
dbSNPrs7968682
ebirs7968682
HLIrs7968682
Exacrs7968682
Varsomers7968682
Maprs7968682
PheGenIrs7968682
hapmaprs7968682
1000 genomesrs7968682
hgdprs7968682
ensemblrs7968682
gopubmedrs7968682
geneviewrs7968682
scholarrs7968682
googlers7968682
pharmgkbrs7968682
gwascentralrs7968682
openSNPrs7968682
23andMers7968682
23andMe allrs7968682
SNP Nexus

SNPshotrs7968682
SNPdbers7968682
MSV3drs7968682
GWAS Ctlgrs7968682
GMAF0.3329
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 22021425OA-icon.png]
Trait
Title Genome-wide association study of body height in African Americans: the Women's Health Initiative SNP Health Association Resource (SHARe).
Risk Allele T
P-val 4E-10
Odds Ratio 0.0430 None


[PMID 18193045OA-icon.png] Common variants in the GDF5-UQCC region are associated with variation in human height.


[PMID 19132395OA-icon.png] Uterine leiomyomata and decreased height: a common HMGA2 predisposition allele.


[PMID 19930247OA-icon.png] HMGA2 is confirmed to be associated with human adult height.