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rs7112925

From SNPedia

Orientationplus
Stabilizedplus
Make rs7112925(C;C)
Make rs7112925(C;T)
Make rs7112925(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position67058689
GeneRHOD
is asnp
is mentioned by
dbSNPrs7112925
ebirs7112925
HLIrs7112925
Exacrs7112925
Varsomers7112925
Maprs7112925
PheGenIrs7112925
hapmaprs7112925
1000 genomesrs7112925
hgdprs7112925
ensemblrs7112925
gopubmedrs7112925
geneviewrs7112925
scholarrs7112925
googlers7112925
pharmgkbrs7112925
gwascentralrs7112925
openSNPrs7112925
23andMers7112925
23andMe allrs7112925
SNP Nexus

SNPshotrs7112925
SNPdbers7112925
MSV3drs7112925
GWAS Ctlgrs7112925
GMAF0.3448
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 9E-10
Odds Ratio 0.0200 [NR] meters decrease