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rs397518481

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397518481(C;T)
Make rs397518481(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position25501230
GeneRARB
is asnp
is mentioned by
dbSNPrs397518481
ebirs397518481
HLIrs397518481
Exacrs397518481
Varsomers397518481
Maprs397518481
PheGenIrs397518481
hapmaprs397518481
1000 genomesrs397518481
hgdprs397518481
ensemblrs397518481
gopubmedrs397518481
geneviewrs397518481
scholarrs397518481
googlers397518481
pharmgkbrs397518481
gwascentralrs397518481
openSNPrs397518481
23andMers397518481
23andMe allrs397518481
SNP Nexus

SNPshotrs397518481
SNPdbers397518481
MSV3drs397518481
GWAS Ctlgrs397518481
Max Magnitude0
ClinVar
Risk rs397518481(T;T)
Alt rs397518481(T;T)
Reference rs397518481(C;C)
Significance Pathogenic
Disease Microphthalmia
Variation info
Gene RARB
CLNDBN Microphthalmia, syndromic 12
Reversed 0
HGVS NC_000003.11:g.25542721C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000074410.25,