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rs4605213

From SNPedia

Orientationplus
Stabilizedplus
Make rs4605213(C;C)
Make rs4605213(C;G)
Make rs4605213(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position51167386
GeneNME1-NME2, NME2
is asnp
is mentioned by
dbSNPrs4605213
ebirs4605213
HLIrs4605213
Exacrs4605213
Varsomers4605213
Maprs4605213
PheGenIrs4605213
hapmaprs4605213
1000 genomesrs4605213
hgdprs4605213
ensemblrs4605213
gopubmedrs4605213
geneviewrs4605213
scholarrs4605213
googlers4605213
pharmgkbrs4605213
gwascentralrs4605213
openSNPrs4605213
23andMers4605213
23andMe allrs4605213
SNP Nexus

SNPshotrs4605213
SNPdbers4605213
MSV3drs4605213
GWAS Ctlgrs4605213
GMAF0.4412
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 3E-8
Odds Ratio .02 [NR] unit increase