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rs863225435

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs863225435(-;-)
Make rs863225435(-;TC)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position110688774
GeneCHRDL1
is asnp
is mentioned by
dbSNPrs863225435
dbSNP (classic)rs863225435
ClinGenrs863225435
ebirs863225435
HLIrs863225435
Exacrs863225435
Gnomadrs863225435
Varsomers863225435
LitVarrs863225435
Maprs863225435
PheGenIrs863225435
Biobankrs863225435
1000 genomesrs863225435
hgdprs863225435
ensemblrs863225435
geneviewrs863225435
scholarrs863225435
googlers863225435
pharmgkbrs863225435
gwascentralrs863225435
openSNPrs863225435
23andMers863225435
SNPshotrs863225435
SNPdbers863225435
MSV3drs863225435
GWAS Ctlgrs863225435
Max Magnitude0
ClinVar
Risk rs863225435(-;-)
Alt rs863225435(-;-)
Reference Rs863225435(TC;TC)
Significance Pathogenic
Disease Megalocornea
Variation info
Gene CHRDL1
CLNDBN Megalocornea
Reversed 1
HGVS NC_000023.10:g.109932002_109932003delGA
CLNSRC OMIM Allelic Variant
CLNACC RCV000202388.2,