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rs587777664

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587777664(A;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position68231532
GeneATOH7
is asnp
is mentioned by
dbSNPrs587777664
ebirs587777664
HLIrs587777664
Exacrs587777664
Varsomers587777664
Maprs587777664
PheGenIrs587777664
hapmaprs587777664
1000 genomesrs587777664
hgdprs587777664
ensemblrs587777664
gopubmedrs587777664
geneviewrs587777664
scholarrs587777664
googlers587777664
pharmgkbrs587777664
gwascentralrs587777664
openSNPrs587777664
23andMers587777664
23andMe allrs587777664
SNP Nexus

SNPshotrs587777664
SNPdbers587777664
MSV3drs587777664
GWAS Ctlgrs587777664
Max Magnitude0
ClinVar
Risk rs587777664(T;T)
Alt rs587777664(T;T)
Reference rs587777664(A;A)
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.69991289T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000133577.2,