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rs80358299

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80358299(C;C)
Make rs80358299(C;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position86951282
GeneFZD4
is asnp
is mentioned by
dbSNPrs80358299
ebirs80358299
HLIrs80358299
Exacrs80358299
Varsomers80358299
Maprs80358299
PheGenIrs80358299
hapmaprs80358299
1000 genomesrs80358299
hgdprs80358299
ensemblrs80358299
gopubmedrs80358299
geneviewrs80358299
scholarrs80358299
googlers80358299
pharmgkbrs80358299
gwascentralrs80358299
openSNPrs80358299
23andMers80358299
23andMe allrs80358299
SNP Nexus

SNPshotrs80358299
SNPdbers80358299
MSV3drs80358299
GWAS Ctlgrs80358299
Max Magnitude0
ClinVar
Risk rs80358299(C;C)
Alt rs80358299(C;C)
Reference rs80358299(G;G)
Significance Pathogenic
Disease Familial exudative vitreoretinopathy
Variation info
Gene FZD4
CLNDBN Familial exudative vitreoretinopathy
Reversed 1
HGVS NC_000011.9:g.86662324C>G
CLNSRC
CLNACC