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

rs397518482

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397518482(-;-)
Make rs397518482(-;TC)
Make rs397518482(TC;TC)
ReferenceGRCh38 38.1/141
Chromosome3
Position25596475
GeneRARB
is asnp
is mentioned by
dbSNPrs397518482
ebirs397518482
HLIrs397518482
Exacrs397518482
Varsomers397518482
Maprs397518482
PheGenIrs397518482
hapmaprs397518482
1000 genomesrs397518482
hgdprs397518482
ensemblrs397518482
gopubmedrs397518482
geneviewrs397518482
scholarrs397518482
googlers397518482
pharmgkbrs397518482
gwascentralrs397518482
openSNPrs397518482
23andMers397518482
23andMe allrs397518482
SNP Nexus

SNPshotrs397518482
SNPdbers397518482
MSV3drs397518482
GWAS Ctlgrs397518482
Max Magnitude0
ClinVar
Risk rs397518482(CT;CT)
Alt rs397518482(CT;CT)
Reference rs397518482(;)
Significance Pathogenic
Disease Microphthalmia
Variation info
Gene RARB
CLNDBN Microphthalmia, syndromic 12
Reversed 0
HGVS NC_000003.11:g.25637965_25637966dupTC
CLNSRC OMIM Allelic Variant
CLNACC RCV000074411.27,