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rs17081935

From SNPedia

Orientationplus
Stabilizedplus
Make rs17081935(C;C)
Make rs17081935(C;T)
Make rs17081935(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position56957310
is asnp
is mentioned by
dbSNPrs17081935
ebirs17081935
HLIrs17081935
Exacrs17081935
Varsomers17081935
Maprs17081935
PheGenIrs17081935
hapmaprs17081935
1000 genomesrs17081935
hgdprs17081935
ensemblrs17081935
gopubmedrs17081935
geneviewrs17081935
scholarrs17081935
googlers17081935
pharmgkbrs17081935
gwascentralrs17081935
openSNPrs17081935
23andMers17081935
23andMe allrs17081935
SNP Nexus

SNPshotrs17081935
SNPdbers17081935
MSV3drs17081935
GWAS Ctlgrs17081935
GMAF0.2176
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20881960OA-icon.png]
Trait
Title Hundreds of variants clustered in genomic loci and biological pathways affect human height.
Risk Allele T
P-val 4E-11
Odds Ratio 0.0300 [NR] meters increase