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rs869025222

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869025222(C;C)
Make rs869025222(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position25580574
GeneRARB
is asnp
is mentioned by
dbSNPrs869025222
ebirs869025222
HLIrs869025222
Exacrs869025222
Varsomers869025222
Maprs869025222
PheGenIrs869025222
hapmaprs869025222
1000 genomesrs869025222
hgdprs869025222
ensemblrs869025222
gopubmedrs869025222
geneviewrs869025222
scholarrs869025222
googlers869025222
pharmgkbrs869025222
gwascentralrs869025222
openSNPrs869025222
23andMers869025222
23andMe allrs869025222
SNP Nexus

SNPshotrs869025222
SNPdbers869025222
MSV3drs869025222
GWAS Ctlgrs869025222
Max Magnitude0
ClinVar
Risk rs869025222(C;C)
Alt rs869025222(C;C)
Reference rs869025222(T;T)
Significance Probable-Pathogenic
Disease Microphthalmia
Variation info
Gene RARB
CLNDBN Microphthalmia, syndromic 12
Reversed 0
HGVS NC_000003.11:g.25622065T>C
CLNSRC
CLNACC RCV000207485.1,