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rs10906982

From SNPedia

Orientationplus
Stabilizedplus
Make rs10906982(A;A)
Make rs10906982(A;T)
Make rs10906982(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position83899406
GeneADAMTSL3
is asnp
is mentioned by
dbSNPrs10906982
ebirs10906982
HLIrs10906982
Exacrs10906982
Varsomers10906982
Maprs10906982
PheGenIrs10906982
hapmaprs10906982
1000 genomesrs10906982
hgdprs10906982
ensemblrs10906982
gopubmedrs10906982
geneviewrs10906982
scholarrs10906982
googlers10906982
pharmgkbrs10906982
gwascentralrs10906982
openSNPrs10906982
23andMers10906982
23andMe allrs10906982
SNP Nexus

SNPshotrs10906982
SNPdbers10906982
MSV3drs10906982
GWAS Ctlgrs10906982
GMAF0.3274
Max Magnitude
? (A;A) (A;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 A
P-val 2E-8
Odds Ratio 0.05 [0.02-0.07] SD taller - among males
GWAS snp
PMID [PMID 20397748OA-icon.png]
Trait Height
Title Genome-Wide Association Study of Height and Body Mass Index in Australian Twin Families
Risk Allele A
P-val 5E-7
Odds Ratio 0.07 [0.03-0.11] SD increase


[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
rs10906982
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.726562
summary