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rs17032362

From SNPedia

Orientationplus
Stabilizedplus
Make rs17032362(A;A)
Make rs17032362(A;G)
Make rs17032362(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position102236525
is asnp
is mentioned by
dbSNPrs17032362
dbSNP (classic)rs17032362
ClinGenrs17032362
ebirs17032362
HLIrs17032362
Exacrs17032362
Gnomadrs17032362
Varsomers17032362
LitVarrs17032362
Maprs17032362
PheGenIrs17032362
Biobankrs17032362
1000 genomesrs17032362
hgdprs17032362
ensemblrs17032362
geneviewrs17032362
scholarrs17032362
googlers17032362
pharmgkbrs17032362
gwascentralrs17032362
openSNPrs17032362
23andMers17032362
SNPshotrs17032362
SNPdbers17032362
MSV3drs17032362
GWAS Ctlgrs17032362
GMAF0.1015
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 22503243] Replication study of the association of SNPs in the LHX3-QSOX2 and IGF1 loci with adult height in the Japanese population; wide-ranging comparison of each SNP genotype distribution [PMID 20189936] A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci.


[PMID 22689104] No effect of the IGF-1 gene rs35767 and rs17032362 polymorphisms in the etiology of idiopathic short stature.