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rs10935120

From SNPedia

Orientationplus
Stabilizedplus
Make rs10935120(A;A)
Make rs10935120(A;G)
Make rs10935120(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position134514250
GeneCEP63
is asnp
is mentioned by
dbSNPrs10935120
ebirs10935120
HLIrs10935120
Exacrs10935120
Varsomers10935120
Maprs10935120
PheGenIrs10935120
hapmaprs10935120
1000 genomesrs10935120
hgdprs10935120
ensemblrs10935120
gopubmedrs10935120
geneviewrs10935120
scholarrs10935120
googlers10935120
pharmgkbrs10935120
gwascentralrs10935120
openSNPrs10935120
23andMers10935120
23andMe allrs10935120
SNP Nexus

SNPshotrs10935120
SNPdbers10935120
MSV3drs10935120
GWAS Ctlgrs10935120
GMAF0.3196
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 18391952OA-icon.png]
Trait Height
Title Genome-wide association analysis identifies 20 loci that influence adult height
Risk Allele A
P-val 7.0000000000000005E-8
Odds Ratio 0.06 [0.03-0.09] SD shorter - among males


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


[PMID 19557189OA-icon.png] Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions.


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


GET Evidence
rs10935120
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.507812
summary