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rs17511102

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs17511102(A;T)
Make rs17511102(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position37733470
is asnp
is mentioned by
dbSNPrs17511102
ebirs17511102
HLIrs17511102
Exacrs17511102
Varsomers17511102
Maprs17511102
PheGenIrs17511102
hapmaprs17511102
1000 genomesrs17511102
hgdprs17511102
ensemblrs17511102
gopubmedrs17511102
geneviewrs17511102
scholarrs17511102
googlers17511102
pharmgkbrs17511102
gwascentralrs17511102
openSNPrs17511102
23andMers17511102
23andMe allrs17511102
SNP Nexus

SNPshotrs17511102
SNPdbers17511102
MSV3drs17511102
GWAS Ctlgrs17511102
GMAF0.02938
Max Magnitude0
? (A;A) (A;T) (T;T) 28
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 A
P-val 2E-18
Odds Ratio 0.06 [NR] unit decrease
GWAS snp
PMID [PMID 23563607OA-icon.png]
Trait Height
Title Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.
Risk Allele T
P-val 2E-8
Odds Ratio 1.40 [NR]