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rs7744813

From SNPedia

Orientationplus
Stabilizedplus
Make rs7744813(A;A)
Make rs7744813(A;C)
Make rs7744813(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position72933566
GeneKCNQ5
is asnp
is mentioned by
dbSNPrs7744813
ebirs7744813
HLIrs7744813
Exacrs7744813
Varsomers7744813
Maprs7744813
PheGenIrs7744813
hapmaprs7744813
1000 genomesrs7744813
hgdprs7744813
ensemblrs7744813
gopubmedrs7744813
geneviewrs7744813
scholarrs7744813
googlers7744813
pharmgkbrs7744813
gwascentralrs7744813
openSNPrs7744813
23andMers7744813
23andMe allrs7744813
SNP Nexus

SNPshotrs7744813
SNPdbers7744813
MSV3drs7744813
GWAS Ctlgrs7744813
GMAF0.2851
Max Magnitude
? (A;A) (A;C) (C;C) 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 C
P-val 4E-9
Odds Ratio .11 [0.075-0.149] unit increase