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rs80358297

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80358297(A;C)
Make rs80358297(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position86951423
GeneFZD4, PRSS23
is asnp
is mentioned by
dbSNPrs80358297
dbSNP (classic)rs80358297
ClinGenrs80358297
ebirs80358297
HLIrs80358297
Exacrs80358297
Gnomadrs80358297
Varsomers80358297
LitVarrs80358297
Maprs80358297
PheGenIrs80358297
Biobankrs80358297
1000 genomesrs80358297
hgdprs80358297
ensemblrs80358297
geneviewrs80358297
scholarrs80358297
googlers80358297
pharmgkbrs80358297
gwascentralrs80358297
openSNPrs80358297
23andMers80358297
SNPshotrs80358297
SNPdbers80358297
MSV3drs80358297
GWAS Ctlgrs80358297
Max Magnitude0
ClinVar
Risk rs80358297(C;C)
Alt rs80358297(C;C)
Reference Rs80358297(A;A)
Significance Pathogenic
Disease Familial exudative vitreoretinopathy
Variation info
Gene FZD4
CLNDBN Familial exudative vitreoretinopathy
Reversed 1
HGVS NC_000011.9:g.86662465T>G
CLNSRC
CLNACC