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rs9967417

From SNPedia

Orientationplus
Stabilizedplus
Make rs9967417(C;C)
Make rs9967417(C;G)
Make rs9967417(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position49433130
GeneDYM
is asnp
is mentioned by
dbSNPrs9967417
ebirs9967417
HLIrs9967417
Exacrs9967417
Varsomers9967417
Maprs9967417
PheGenIrs9967417
hapmaprs9967417
1000 genomesrs9967417
hgdprs9967417
ensemblrs9967417
gopubmedrs9967417
geneviewrs9967417
scholarrs9967417
googlers9967417
pharmgkbrs9967417
gwascentralrs9967417
openSNPrs9967417
23andMers9967417
23andMe allrs9967417
SNP Nexus

SNPshotrs9967417
SNPdbers9967417
MSV3drs9967417
GWAS Ctlgrs9967417
GMAF0.2218
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 9E-25
Odds Ratio .04 [NR] unit decrease
GWAS snp
PMID [PMID 23563607OA-icon.png]
Trait Height
Title Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.
Risk Allele G
P-val 5E-9
Odds Ratio 1.13 [NR]