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rs2665838

From SNPedia

Orientationminus
Stabilizedminus
Make rs2665838(C;C)
Make rs2665838(C;G)
Make rs2665838(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position63889105
is asnp
is mentioned by
dbSNPrs2665838
ebirs2665838
HLIrs2665838
Exacrs2665838
Varsomers2665838
Maprs2665838
PheGenIrs2665838
hapmaprs2665838
1000 genomesrs2665838
hgdprs2665838
ensemblrs2665838
gopubmedrs2665838
geneviewrs2665838
scholarrs2665838
googlers2665838
pharmgkbrs2665838
gwascentralrs2665838
openSNPrs2665838
23andMers2665838
23andMe allrs2665838
SNP Nexus

SNPshotrs2665838
SNPdbers2665838
MSV3drs2665838
GWAS Ctlgrs2665838
GMAF0.1901
Max Magnitude
? (C;C) (C;G) (G;G) 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 C
P-val 5E-25
Odds Ratio 0.04 [NR] unit decrease