Have questions? Visit https://www.reddit.com/r/SNPedia

rs61735304

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61735304(A;A)
Make rs61735304(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position86954989
GeneCSF2RB, FZD4
is asnp
is mentioned by
dbSNPrs61735304
ebirs61735304
HLIrs61735304
Exacrs61735304
Varsomers61735304
Maprs61735304
PheGenIrs61735304
hapmaprs61735304
1000 genomesrs61735304
hgdprs61735304
ensemblrs61735304
gopubmedrs61735304
geneviewrs61735304
scholarrs61735304
googlers61735304
pharmgkbrs61735304
gwascentralrs61735304
openSNPrs61735304
23andMers61735304
23andMe allrs61735304
SNP Nexus

SNPshotrs61735304
SNPdbers61735304
MSV3drs61735304
GWAS Ctlgrs61735304
GMAF0.009183
Max Magnitude0
ClinVar
Risk rs61735304(A;A)
Alt rs61735304(A;A)
Reference rs61735304(G;G)
Significance Non-pathogenic
Disease not specified
Variation info
Gene FZD4 LOC100506368
CLNDBN not specified
Reversed 0
HGVS NC_000011.9:g.86666031G>A
CLNSRC
CLNACC RCV000173423.1,


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


[PMID 17093393] Identification of novel FZD4 mutations in Indian patients with familial exudative vitreoretinopathy.