Rs11190870

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Orientationplus
Make rs11190870(C;C)
Make rs11190870(C;T)
Make rs11190870(T;T)
ReferenceGRCh37 37.1/132
Chromosome10
Position102979207
is asnp
is mentioned by
dbSNPrs11190870
PheGenIrs11190870
nextbiors11190870
hapmaprs11190870
1000 genomesrs11190870
hgdprs11190870
ensemblrs11190870
gopubmedrs11190870
geneviewrs11190870
scholarrs11190870
googlers11190870
pharmgkbrs11190870
gwascentralrs11190870
openSNPrs11190870
23andMers11190870
23andMe allrs11190870
SNP Nexus

SNPshotrs11190870
SNPdbers11190870
MSV3drs11190870
GMAF0.4238
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 21331621] Genetic variants in ultraconserved elements and risk of breast cancer in Chinese population

The T allele of this SNP is associated with an increased risk of scoliosis in adolescent Japanese girls. [1]

GWAS snp
PMID [PMID 22019779]
Trait
Title A genome-wide association study identifies common variants near LBX1 associated with adolescent idiopathic scoliosis.
Risk Allele
P-val 1E-19
Odds Ratio 1.5600 None


[PMID 23096252OA-icon.png] Association of rs11190870 near LBX1 with adolescent idiopathic scoliosis susceptibility in a Han Chinese population.


[PMID 24878781] Association of rs11190870 near LBX1 with adolescent idiopathic scoliosis in East Asians: a systematic review and meta-analysis