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rs7571816

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs7571816(A;G)
Make rs7571816(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position232212354
GeneDIS3L2
is asnp
is mentioned by
dbSNPrs7571816
dbSNP (classic)rs7571816
ClinGenrs7571816
ebirs7571816
HLIrs7571816
Exacrs7571816
Gnomadrs7571816
Varsomers7571816
LitVarrs7571816
Maprs7571816
PheGenIrs7571816
Biobankrs7571816
1000 genomesrs7571816
hgdprs7571816
ensemblrs7571816
geneviewrs7571816
scholarrs7571816
googlers7571816
pharmgkbrs7571816
gwascentralrs7571816
openSNPrs7571816
23andMers7571816
SNPshotrs7571816
SNPdbers7571816
MSV3drs7571816
GWAS Ctlgrs7571816
GMAF0.1965
Max Magnitude0
? (A;A) (A;G) (G;G) 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 A
P-val 9E-9
Odds Ratio 0.06 [0.04-0.08] cm increase