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rs2070776

From SNPedia

Orientationminus
Stabilizedminus
Make rs2070776(C;C)
Make rs2070776(C;T)
Make rs2070776(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position63930138
GeneCD79B
is asnp
is mentioned by
dbSNPrs2070776
ebirs2070776
HLIrs2070776
Exacrs2070776
Varsomers2070776
Maprs2070776
PheGenIrs2070776
hapmaprs2070776
1000 genomesrs2070776
hgdprs2070776
ensemblrs2070776
gopubmedrs2070776
geneviewrs2070776
scholarrs2070776
googlers2070776
pharmgkbrs2070776
gwascentralrs2070776
openSNPrs2070776
23andMers2070776
23andMe allrs2070776
SNP Nexus

SNPshotrs2070776
SNPdbers2070776
MSV3drs2070776
GWAS Ctlgrs2070776
GMAF0.4013
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
P-val 9E-9
Odds Ratio NR NR