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rs891088

From SNPedia

Orientationplus
Stabilizedplus
Make rs891088(A;A)
Make rs891088(A;G)
Make rs891088(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position7184751
GeneINSR
is asnp
is mentioned by
dbSNPrs891088
ebirs891088
HLIrs891088
Exacrs891088
Varsomers891088
Maprs891088
PheGenIrs891088
hapmaprs891088
1000 genomesrs891088
hgdprs891088
ensemblrs891088
gopubmedrs891088
geneviewrs891088
scholarrs891088
googlers891088
pharmgkbrs891088
gwascentralrs891088
openSNPrs891088
23andMers891088
23andMe allrs891088
SNP Nexus

SNPshotrs891088
SNPdbers891088
MSV3drs891088
GWAS Ctlgrs891088
GMAF0.3007
Max Magnitude
? (A;A) (A;G) (G;G) 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 A
P-val 2E-12
Odds Ratio 0.0300 [NR] meters decrease