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rs7853377

From SNPedia

Orientationplus
Stabilizedplus
Make rs7853377(A;A)
Make rs7853377(A;G)
Make rs7853377(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position83937290
is asnp
is mentioned by
dbSNPrs7853377
ebirs7853377
HLIrs7853377
Exacrs7853377
Varsomers7853377
Maprs7853377
PheGenIrs7853377
hapmaprs7853377
1000 genomesrs7853377
hgdprs7853377
ensemblrs7853377
gopubmedrs7853377
geneviewrs7853377
scholarrs7853377
googlers7853377
pharmgkbrs7853377
gwascentralrs7853377
openSNPrs7853377
23andMers7853377
23andMe allrs7853377
SNP Nexus

SNPshotrs7853377
SNPdbers7853377
MSV3drs7853377
GWAS Ctlgrs7853377
GMAF0.1795
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 5E-8
Odds Ratio .02 [NR] unit decrease