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rs7829127

From SNPedia

Orientationplus
Stabilizedplus
Make rs7829127(A;A)
Make rs7829127(A;G)
Make rs7829127(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position40868875
GeneZMAT4
is asnp
is mentioned by
dbSNPrs7829127
dbSNP (classic)rs7829127
ClinGenrs7829127
ebirs7829127
HLIrs7829127
Exacrs7829127
Gnomadrs7829127
Varsomers7829127
LitVarrs7829127
Maprs7829127
PheGenIrs7829127
Biobankrs7829127
1000 genomesrs7829127
hgdprs7829127
ensemblrs7829127
geneviewrs7829127
scholarrs7829127
googlers7829127
pharmgkbrs7829127
gwascentralrs7829127
openSNPrs7829127
23andMers7829127
SNPshotrs7829127
SNPdbers7829127
MSV3drs7829127
GWAS Ctlgrs7829127
GMAF0.213
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 23396134OA-icon.png]
Trait Refractive error
Title Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.
Risk Allele G
P-val 4E-10
Odds Ratio .12 [0.081-0.151] unit increase