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rs10770705

From SNPedia

Orientationplus
Stabilizedplus
Make rs10770705(A;A)
Make rs10770705(A;C)
Make rs10770705(C;C)
ReferenceGRCh38 38.1/141
Chromosome12
Position20704533
GeneSLCO1C1
is asnp
is mentioned by
dbSNPrs10770705
ebirs10770705
HLIrs10770705
Exacrs10770705
Varsomers10770705
Maprs10770705
PheGenIrs10770705
hapmaprs10770705
1000 genomesrs10770705
hgdprs10770705
ensemblrs10770705
gopubmedrs10770705
geneviewrs10770705
scholarrs10770705
googlers10770705
pharmgkbrs10770705
gwascentralrs10770705
openSNPrs10770705
23andMers10770705
23andMe allrs10770705
SNP Nexus

SNPshotrs10770705
SNPdbers10770705
MSV3drs10770705
GWAS Ctlgrs10770705
GMAF0.2713
Max Magnitude
? (A;A) (A;C) (C;C) 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 8E-18
Odds Ratio 0.03 [NR] unit increase