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rs17346452

From SNPedia

Orientationplus
Stabilizedplus
Make rs17346452(C;C)
Make rs17346452(C;T)
Make rs17346452(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position172084147
GeneDNM3
is asnp
is mentioned by
dbSNPrs17346452
ebirs17346452
HLIrs17346452
Exacrs17346452
Varsomers17346452
Maprs17346452
PheGenIrs17346452
hapmaprs17346452
1000 genomesrs17346452
hgdprs17346452
ensemblrs17346452
gopubmedrs17346452
geneviewrs17346452
scholarrs17346452
googlers17346452
pharmgkbrs17346452
gwascentralrs17346452
openSNPrs17346452
23andMers17346452
23andMe allrs17346452
SNP Nexus

SNPshotrs17346452
SNPdbers17346452
MSV3drs17346452
GWAS Ctlgrs17346452
GMAF0.1148
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 T
P-val 1E-23
Odds Ratio .04 [NR] unit decrease