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rs2778031

From SNPedia

Orientationplus
Stabilizedplus
Make rs2778031(C;C)
Make rs2778031(C;T)
Make rs2778031(T;T)
ReferenceGRCh37 37.1/132
Chromosome9
Position88220811
GeneLOC100129340
is asnp
is mentioned by
dbSNPrs2778031
dbSNP (classic)rs2778031
ClinGenrs2778031
ebirs2778031
HLIrs2778031
Exacrs2778031
Gnomadrs2778031
Varsomers2778031
LitVarrs2778031
Maprs2778031
PheGenIrs2778031
Biobankrs2778031
1000 genomesrs2778031
hgdprs2778031
ensemblrs2778031
geneviewrs2778031
scholarrs2778031
googlers2778031
pharmgkbrs2778031
gwascentralrs2778031
openSNPrs2778031
23andMers2778031
SNPshotrs2778031
SNPdbers2778031
MSV3drs2778031
GWAS Ctlgrs2778031
GMAF0.4729
Max Magnitude0
? (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 T
P-val 9E-13
Odds Ratio 0.03 [NR] unit increase