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rs587777625

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777625(C;C)
Make rs587777625(C;T)
ReferenceGRCh38 38.1/142
Chromosome12
Position56235666
GeneSLC39A5
is asnp
is mentioned by
dbSNPrs587777625
ebirs587777625
HLIrs587777625
Exacrs587777625
Varsomers587777625
Maprs587777625
PheGenIrs587777625
hapmaprs587777625
1000 genomesrs587777625
hgdprs587777625
ensemblrs587777625
gopubmedrs587777625
geneviewrs587777625
scholarrs587777625
googlers587777625
pharmgkbrs587777625
gwascentralrs587777625
openSNPrs587777625
23andMers587777625
23andMe allrs587777625
SNP Nexus

SNPshotrs587777625
SNPdbers587777625
MSV3drs587777625
GWAS Ctlgrs587777625
Max Magnitude0
ClinVar
Risk rs587777625(C;C)
Alt rs587777625(C;C)
Reference rs587777625(T;T)
Significance Pathogenic
Disease Myopia 24
Variation info
Gene SLC39A5
CLNDBN Myopia 24, autosomal dominant
Reversed 0
HGVS NC_000012.11:g.56629450T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000133507.2,