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rs104894223

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104894223(A;G)
Make rs104894223(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position86951990
GeneFZD4
is asnp
is mentioned by
dbSNPrs104894223
ebirs104894223
HLIrs104894223
Exacrs104894223
Varsomers104894223
Maprs104894223
PheGenIrs104894223
hapmaprs104894223
1000 genomesrs104894223
hgdprs104894223
ensemblrs104894223
gopubmedrs104894223
geneviewrs104894223
scholarrs104894223
googlers104894223
pharmgkbrs104894223
gwascentralrs104894223
openSNPrs104894223
23andMers104894223
23andMe allrs104894223
SNP Nexus

SNPshotrs104894223
SNPdbers104894223
MSV3drs104894223
GWAS Ctlgrs104894223
Max Magnitude0
OMIM604579
Desc
Variant0006
Relatedalso
ClinVar
Risk rs104894223(G;G)
Alt rs104894223(G;G)
Reference rs104894223(A;A)
Significance Pathogenic
Disease Retinopathy of prematurity
Variation info
Gene PRSS23 FZD4
CLNDBN Retinopathy of prematurity
Reversed 1
HGVS NC_000011.9:g.86663032T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000005824.2,