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rs387906713

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906713(G;T)
Make rs387906713(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position110688800
GeneCHRDL1
is asnp
is mentioned by
dbSNPrs387906713
ebirs387906713
HLIrs387906713
Exacrs387906713
Varsomers387906713
Maprs387906713
PheGenIrs387906713
hapmaprs387906713
1000 genomesrs387906713
hgdprs387906713
ensemblrs387906713
gopubmedrs387906713
geneviewrs387906713
scholarrs387906713
googlers387906713
pharmgkbrs387906713
gwascentralrs387906713
openSNPrs387906713
23andMers387906713
23andMe allrs387906713
SNP Nexus

SNPshotrs387906713
SNPdbers387906713
MSV3drs387906713
GWAS Ctlgrs387906713
Max Magnitude0
ClinVar
Risk rs387906713(T;T)
Alt rs387906713(T;T)
Reference rs387906713(G;G)
Significance Pathogenic
Disease Megalocornea
Variation info
Gene CHRDL1
CLNDBN Megalocornea
Reversed 1
HGVS NC_000023.10:g.109932028C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000022850.4,