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rs1741344

From SNPedia

Orientationplus
Stabilizedplus
Make rs1741344(C;C)
Make rs1741344(C;T)
Make rs1741344(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position4121153
GeneLOC101929155
is asnp
is mentioned by
dbSNPrs1741344
ebirs1741344
HLIrs1741344
Exacrs1741344
Varsomers1741344
Maprs1741344
PheGenIrs1741344
hapmaprs1741344
1000 genomesrs1741344
hgdprs1741344
ensemblrs1741344
gopubmedrs1741344
geneviewrs1741344
scholarrs1741344
googlers1741344
pharmgkbrs1741344
gwascentralrs1741344
openSNPrs1741344
23andMers1741344
23andMe allrs1741344
SNP Nexus

SNPshotrs1741344
SNPdbers1741344
MSV3drs1741344
GWAS Ctlgrs1741344
GMAF0.3053
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20881960OA-icon.png]
Trait
Title Hundreds of variants clustered in genomic loci and biological pathways affect human height.
Risk Allele T
P-val 3E-9
Odds Ratio 0.0200 [NR] meters decrease