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rs16859517

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs16859517(C;T)
Make rs16859517(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position219084462
GeneNHEJ1
is asnp
is mentioned by
dbSNPrs16859517
dbSNP (classic)rs16859517
ClinGenrs16859517
ebirs16859517
HLIrs16859517
Exacrs16859517
Gnomadrs16859517
Varsomers16859517
LitVarrs16859517
Maprs16859517
PheGenIrs16859517
Biobankrs16859517
1000 genomesrs16859517
hgdprs16859517
ensemblrs16859517
geneviewrs16859517
scholarrs16859517
googlers16859517
pharmgkbrs16859517
gwascentralrs16859517
openSNPrs16859517
23andMers16859517
SNPshotrs16859517
SNPdbers16859517
MSV3drs16859517
GWAS Ctlgrs16859517
GMAF0.1653
Max Magnitude0
? (C;C) (C;T) (T;T) 28



[PMID 28146470OA-icon.png] Rare and low-frequency coding variants alter human adult height.

GWAS snp
PMID [PMID 20189936]
Trait Height
Title A genome-wide association study in 19,633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci
Risk Allele T
P-val 0.000005
Odds Ratio 0.05 [0.03-0.07] cm increase