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rs387906714

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906714(C;T)
Make rs387906714(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position110694289
GeneCHRDL1
is asnp
is mentioned by
dbSNPrs387906714
ebirs387906714
HLIrs387906714
Exacrs387906714
Varsomers387906714
Maprs387906714
PheGenIrs387906714
hapmaprs387906714
1000 genomesrs387906714
hgdprs387906714
ensemblrs387906714
gopubmedrs387906714
geneviewrs387906714
scholarrs387906714
googlers387906714
pharmgkbrs387906714
gwascentralrs387906714
openSNPrs387906714
23andMers387906714
23andMe allrs387906714
SNP Nexus

SNPshotrs387906714
SNPdbers387906714
MSV3drs387906714
GWAS Ctlgrs387906714
Max Magnitude0
ClinVar
Risk rs387906714(T;T)
Alt rs387906714(T;T)
Reference rs387906714(C;C)
Significance Pathogenic
Disease Megalocornea
Variation info
Gene CHRDL1
CLNDBN Megalocornea
Reversed 1
HGVS NC_000023.10:g.109937517G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000022853.13,