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rs4373767

From SNPedia

Orientationplus
Stabilizedplus
Make rs4373767(C;C)
Make rs4373767(C;T)
Make rs4373767(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position219586340
is asnp
is mentioned by
dbSNPrs4373767
ebirs4373767
HLIrs4373767
Exacrs4373767
Varsomers4373767
Maprs4373767
PheGenIrs4373767
hapmaprs4373767
1000 genomesrs4373767
hgdprs4373767
ensemblrs4373767
gopubmedrs4373767
geneviewrs4373767
scholarrs4373767
googlers4373767
pharmgkbrs4373767
gwascentralrs4373767
openSNPrs4373767
23andMers4373767
23andMe allrs4373767
SNP Nexus

SNPshotrs4373767
SNPdbers4373767
MSV3drs4373767
GWAS Ctlgrs4373767
GMAF0.3636
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22685421OA-icon.png]
Trait
Title Genetic variants on chromosome 1q41 influence ocular axial length and high myopia.
Risk Allele C
P-val 3E-10
Odds Ratio 0.1600 None