Rs16896068

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Orientationplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs16896068(A;A)
Make rs16896068(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position17943217
GeneLCORL
is asnp
is mentioned by
dbSNPrs16896068
Exacrs16896068
PheGenIrs16896068
nextbiors16896068
hapmaprs16896068
1000 genomesrs16896068
hgdprs16896068
ensemblrs16896068
gopubmedrs16896068
geneviewrs16896068
scholarrs16896068
googlers16896068
pharmgkbrs16896068
gwascentralrs16896068
openSNPrs16896068
23andMers16896068
23andMe allrs16896068
SNP Nexus

SNPshotrs16896068
SNPdbers16896068
MSV3drs16896068
GMAF0.2259
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS
SNP rs16896068
PubMedID [PMID 18391952OA-icon.png]
Condition Height
Gene LCORL
Risk Allele A
pValue 2.00E-013
OR 0.07
95% CI 0.03-0.11) SD shorter - among male


OMIM612226
DescSTATURE QUANTITATIVE TRAIT LOCUS 13; STQTL13
Variant
Relatedalso
[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.


[PMID 20027299OA-icon.png] Transferability and fine-mapping of genome-wide associated loci for adult height across human populations.


GET Evidence
rs16896068
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.289062
summary