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rs7498403

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs7498403(C;C)
Make rs7498403(C;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position79551124
is asnp
is mentioned by
dbSNPrs7498403
ebirs7498403
HLIrs7498403
Exacrs7498403
Varsomers7498403
Maprs7498403
PheGenIrs7498403
hapmaprs7498403
1000 genomesrs7498403
hgdprs7498403
ensemblrs7498403
gopubmedrs7498403
geneviewrs7498403
scholarrs7498403
googlers7498403
pharmgkbrs7498403
gwascentralrs7498403
openSNPrs7498403
23andMers7498403
23andMe allrs7498403
SNP Nexus

SNPshotrs7498403
SNPdbers7498403
MSV3drs7498403
GWAS Ctlgrs7498403
GMAF0.1318
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20668459]
Trait
Title Genetic variants that affect length/height in infancy/early childhood in Vietnamese-Korean families
Risk Allele C
P-val 0.000005
Odds Ratio None None