Have questions? Visit https://www.reddit.com/r/SNPedia

rs2814993

From SNPedia

Orientationplus
Stabilizedplus
Make rs2814993(A;A)
Make rs2814993(A;G)
Make rs2814993(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position34651116
GeneC6orf106
is asnp
is mentioned by
dbSNPrs2814993
ebirs2814993
HLIrs2814993
Exacrs2814993
Varsomers2814993
Maprs2814993
PheGenIrs2814993
hapmaprs2814993
1000 genomesrs2814993
hgdprs2814993
ensemblrs2814993
gopubmedrs2814993
geneviewrs2814993
scholarrs2814993
googlers2814993
pharmgkbrs2814993
gwascentralrs2814993
openSNPrs2814993
23andMers2814993
23andMe allrs2814993
SNP Nexus

SNPshotrs2814993
SNPdbers2814993
MSV3drs2814993
GWAS Ctlgrs2814993
GMAF0.1116
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 3.9999999999999999E-12
Odds Ratio 0.09 [0.05-0.13] SD taller - among males


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


[PMID 19343178OA-icon.png] Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size.


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


[PMID 20546612OA-icon.png] The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature.


GET Evidence
rs2814993
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.132812
summary