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rs3116602

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common on affy axiom data
Make rs3116602(G;G)
Make rs3116602(G;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position50537219
is asnp
is mentioned by
dbSNPrs3116602
ebirs3116602
HLIrs3116602
Exacrs3116602
Varsomers3116602
Maprs3116602
PheGenIrs3116602
hapmaprs3116602
1000 genomesrs3116602
hgdprs3116602
ensemblrs3116602
gopubmedrs3116602
geneviewrs3116602
scholarrs3116602
googlers3116602
pharmgkbrs3116602
gwascentralrs3116602
openSNPrs3116602
23andMers3116602
23andMe allrs3116602
SNP Nexus

SNPshotrs3116602
SNPdbers3116602
MSV3drs3116602
GWAS Ctlgrs3116602
GMAF0.1056
Max Magnitude0
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 18391952OA-icon.png]
Trait Height
Title Genome-wide association analysis identifies 20 loci that influence adult height
Risk Allele G
P-val 6.9999999999999998E-9
Odds Ratio 0.04 [0.00-0.07] SD shorter - among males


[PMID 19030899OA-icon.png] Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci.


[PMID 20017971OA-icon.png] Assessing the impact of global versus local ancestry in association studies.


GET Evidence
rs3116602
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.117188
summary