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rs11107116

From SNPedia

Orientationplus
Stabilizedplus
Make rs11107116(G;G)
Make rs11107116(G;T)
Make rs11107116(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position93584728
GeneSOCS2
is asnp
is mentioned by
dbSNPrs11107116
ebirs11107116
HLIrs11107116
Exacrs11107116
Varsomers11107116
Maprs11107116
PheGenIrs11107116
hapmaprs11107116
1000 genomesrs11107116
hgdprs11107116
ensemblrs11107116
gopubmedrs11107116
geneviewrs11107116
scholarrs11107116
googlers11107116
pharmgkbrs11107116
gwascentralrs11107116
openSNPrs11107116
23andMers11107116
23andMe allrs11107116
SNP Nexus

SNPshotrs11107116
SNPdbers11107116
MSV3drs11107116
GWAS Ctlgrs11107116
GMAF0.2163
Max Magnitude
? (G;G) (G;T) (T;T) 28

23andMe blog Each T version rs11107116 was associated with faster growth during infancy, and 4.7 mm of adult height.

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 6E-10
Odds Ratio 0.04 [0.01-0.07] 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
rs11107116
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.132812
summary



GWAS snp
PMID [PMID 20881960OA-icon.png]
Trait Height
Title Hundreds of variants clustered in genomic loci and biological pathways affect human height.
Risk Allele T
P-val 1E-34
Odds Ratio .05 [NR] unit increase