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rs6469937

From SNPedia

Orientationplus
Stabilizedplus
Make rs6469937(A;A)
Make rs6469937(A;G)
Make rs6469937(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position120598198
GeneSNTB1
is asnp
is mentioned by
dbSNPrs6469937
ebirs6469937
HLIrs6469937
Exacrs6469937
Varsomers6469937
Maprs6469937
PheGenIrs6469937
hapmaprs6469937
1000 genomesrs6469937
hgdprs6469937
ensemblrs6469937
gopubmedrs6469937
geneviewrs6469937
scholarrs6469937
googlers6469937
pharmgkbrs6469937
gwascentralrs6469937
openSNPrs6469937
23andMers6469937
23andMe allrs6469937
SNP Nexus

SNPshotrs6469937
SNPdbers6469937
MSV3drs6469937
GWAS Ctlgrs6469937
GMAF0.3972
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23933737]
Trait Myopia (severe)
Title Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia.
Risk Allele A
P-val 2E-9
Odds Ratio 1.27 [NR]