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rs2093210

From SNPedia

Orientationplus
Stabilizedplus
Make rs2093210(C;C)
Make rs2093210(C;T)
Make rs2093210(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position60490561
is asnp
is mentioned by
dbSNPrs2093210
ebirs2093210
HLIrs2093210
Exacrs2093210
Varsomers2093210
Maprs2093210
PheGenIrs2093210
hapmaprs2093210
1000 genomesrs2093210
hgdprs2093210
ensemblrs2093210
gopubmedrs2093210
geneviewrs2093210
scholarrs2093210
googlers2093210
pharmgkbrs2093210
gwascentralrs2093210
openSNPrs2093210
23andMers2093210
23andMe allrs2093210
SNP Nexus

SNPshotrs2093210
SNPdbers2093210
MSV3drs2093210
GWAS Ctlgrs2093210
GMAF0.3838
Max Magnitude
? (C;C) (C;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 T
P-val 6E-17
Odds Ratio 0.03 [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 C
P-val 8E-13
Odds Ratio 1.16 [NR]