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rs398122852

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs398122852(-;-)
Make rs398122852(-;AG)
Make rs398122852(AG;AG)
ReferenceGRCh38 38.1/141
ChromosomeX
Position110762800
GeneCHRDL1
is asnp
is mentioned by
dbSNPrs398122852
ebirs398122852
HLIrs398122852
Exacrs398122852
Varsomers398122852
Maprs398122852
PheGenIrs398122852
hapmaprs398122852
1000 genomesrs398122852
hgdprs398122852
ensemblrs398122852
gopubmedrs398122852
geneviewrs398122852
scholarrs398122852
googlers398122852
pharmgkbrs398122852
gwascentralrs398122852
openSNPrs398122852
23andMers398122852
23andMe allrs398122852
SNP Nexus

SNPshotrs398122852
SNPdbers398122852
MSV3drs398122852
GWAS Ctlgrs398122852
Max Magnitude0
ClinVar
Risk rs398122852(;)
Alt rs398122852(;)
Reference rs398122852(GA;GA)
Significance Pathogenic
Disease Megalocornea
Variation info
Gene CHRDL1
CLNDBN Megalocornea
Reversed 1
HGVS NC_000023.10:g.110006028_110006029delCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000022852.20,