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rs587776868

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587776868(A;C)
Make rs587776868(C;C)
ReferenceGRCh38 38.1/142
ChromosomeX
Position110759659
GeneCHRDL1
is asnp
is mentioned by
dbSNPrs587776868
ebirs587776868
HLIrs587776868
Exacrs587776868
Varsomers587776868
Maprs587776868
PheGenIrs587776868
hapmaprs587776868
1000 genomesrs587776868
hgdprs587776868
ensemblrs587776868
gopubmedrs587776868
geneviewrs587776868
scholarrs587776868
googlers587776868
pharmgkbrs587776868
gwascentralrs587776868
openSNPrs587776868
23andMers587776868
23andMe allrs587776868
SNP Nexus

SNPshotrs587776868
SNPdbers587776868
MSV3drs587776868
GWAS Ctlgrs587776868
Max Magnitude0
ClinVar
Risk rs587776868(A,C;A,C)
Alt rs587776868(A,C;A,C)
Reference rs587776868(T;T)
Significance Pathogenic
Disease Megalocornea
Variation info
Gene CHRDL1
CLNDBN Megalocornea
Reversed 1
HGVS NC_000023.10:g.110002887A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000022851.5,