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rs61735303

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61735303(A;A)
Make rs61735303(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position86952254
GeneFZD4
is asnp
is mentioned by
dbSNPrs61735303
ebirs61735303
HLIrs61735303
Exacrs61735303
Varsomers61735303
Maprs61735303
PheGenIrs61735303
hapmaprs61735303
1000 genomesrs61735303
hgdprs61735303
ensemblrs61735303
gopubmedrs61735303
geneviewrs61735303
scholarrs61735303
googlers61735303
pharmgkbrs61735303
gwascentralrs61735303
openSNPrs61735303
23andMers61735303
23andMe allrs61735303
SNP Nexus

SNPshotrs61735303
SNPdbers61735303
MSV3drs61735303
GWAS Ctlgrs61735303
GMAF0.0101
Max Magnitude0
ClinVar
Risk rs61735303(A;A)
Alt rs61735303(A;A)
Reference rs61735303(G;G)
Significance Pathogenic
Disease Familial exudative vitreoretinopathy
Variation info
Gene FZD4
CLNDBN Familial exudative vitreoretinopathy
Reversed 0
HGVS NC_000011.9:g.86663296G>A
CLNSRC
CLNACC



[PMID 15223780] Spectrum and frequency of FZD4 mutations in familial exudative vitreoretinopathy.


[PMID 15733276] Genetic variants of frizzled-4 gene in familial exudative vitreoretinopathy and advanced retinopathy of prematurity.