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rs587777665

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777665(-;-)
Make rs587777665(-;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position68231625
GeneATOH7
is asnp
is mentioned by
dbSNPrs587777665
ebirs587777665
HLIrs587777665
Exacrs587777665
Varsomers587777665
Maprs587777665
PheGenIrs587777665
hapmaprs587777665
1000 genomesrs587777665
hgdprs587777665
ensemblrs587777665
gopubmedrs587777665
geneviewrs587777665
scholarrs587777665
googlers587777665
pharmgkbrs587777665
gwascentralrs587777665
openSNPrs587777665
23andMers587777665
23andMe allrs587777665
SNP Nexus

SNPshotrs587777665
SNPdbers587777665
MSV3drs587777665
GWAS Ctlgrs587777665
Max Magnitude0
ClinVar
Risk rs587777665(GG,G;GG,G)
Alt rs587777665(GG,G;GG,G)
Reference rs587777665(CG;CG)
Significance Pathogenic
Disease Persistent hyperplastic primary vitreous
Variation info
Gene ATOH7
CLNDBN Persistent hyperplastic primary vitreous, autosomal recessive
Reversed 1
HGVS NC_000010.10:g.69991382delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000133578.2,