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rs2353398

From SNPedia

Orientationplus
Stabilizedplus
Make rs2353398(A;A)
Make rs2353398(A;T)
Make rs2353398(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position144601606
is asnp
is mentioned by
dbSNPrs2353398
ebirs2353398
HLIrs2353398
Exacrs2353398
Varsomers2353398
Maprs2353398
PheGenIrs2353398
hapmaprs2353398
1000 genomesrs2353398
hgdprs2353398
ensemblrs2353398
gopubmedrs2353398
geneviewrs2353398
scholarrs2353398
googlers2353398
pharmgkbrs2353398
gwascentralrs2353398
openSNPrs2353398
23andMers2353398
23andMe allrs2353398
SNP Nexus

SNPshotrs2353398
SNPdbers2353398
MSV3drs2353398
GWAS Ctlgrs2353398
GMAF0.314
Max Magnitude
? (A;A) (A;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
P-val 2E-9
Odds Ratio NR NR