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rs1738475

From SNPedia

Orientationplus
Stabilizedplus
Make rs1738475(C;C)
Make rs1738475(C;G)
Make rs1738475(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position23210398
is asnp
is mentioned by
dbSNPrs1738475
ebirs1738475
HLIrs1738475
Exacrs1738475
Varsomers1738475
Maprs1738475
PheGenIrs1738475
hapmaprs1738475
1000 genomesrs1738475
hgdprs1738475
ensemblrs1738475
gopubmedrs1738475
geneviewrs1738475
scholarrs1738475
googlers1738475
pharmgkbrs1738475
gwascentralrs1738475
openSNPrs1738475
23andMers1738475
23andMe allrs1738475
SNP Nexus

SNPshotrs1738475
SNPdbers1738475
MSV3drs1738475
GWAS Ctlgrs1738475
GMAF0.4972
Max Magnitude
? (C;C) (C;G) (G;G) 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 C
P-val 3E-12
Odds Ratio 0.0300 [NR] meters increase