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rs17780086

From SNPedia

Orientationplus
Stabilizedplus
Make rs17780086(A;A)
Make rs17780086(A;G)
Make rs17780086(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position32016263
is asnp
is mentioned by
dbSNPrs17780086
ebirs17780086
HLIrs17780086
Exacrs17780086
Varsomers17780086
Maprs17780086
PheGenIrs17780086
hapmaprs17780086
1000 genomesrs17780086
hgdprs17780086
ensemblrs17780086
gopubmedrs17780086
geneviewrs17780086
scholarrs17780086
googlers17780086
pharmgkbrs17780086
gwascentralrs17780086
openSNPrs17780086
23andMers17780086
23andMe allrs17780086
SNP Nexus

SNPshotrs17780086
SNPdbers17780086
MSV3drs17780086
GWAS Ctlgrs17780086
GMAF0.06841
Max Magnitude
? (A;A) (A;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 A
P-val 3E-8
Odds Ratio .03 [NR] unit increase