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rs7032940

From SNPedia

Orientationplus
Stabilizedplus
Make rs7032940(A;A)
Make rs7032940(A;G)
Make rs7032940(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position110183125
is asnp
is mentioned by
dbSNPrs7032940
ebirs7032940
HLIrs7032940
Exacrs7032940
Varsomers7032940
Maprs7032940
PheGenIrs7032940
hapmaprs7032940
1000 genomesrs7032940
hgdprs7032940
ensemblrs7032940
gopubmedrs7032940
geneviewrs7032940
scholarrs7032940
googlers7032940
pharmgkbrs7032940
gwascentralrs7032940
openSNPrs7032940
23andMers7032940
23andMe allrs7032940
SNP Nexus

SNPshotrs7032940
SNPdbers7032940
MSV3drs7032940
GWAS Ctlgrs7032940
GMAF0.1915
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19893584]
Trait Height
Title Identification of 15 loci influencing height in a Korean population
Risk Allele A
P-val 0.000003
Odds Ratio 1.32 [NR] cm increase


GET Evidence
rs7032940
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.265625
summary