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rs869025221

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025221(C;C)
Make rs869025221(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position25593603
GeneRARB
is asnp
is mentioned by
dbSNPrs869025221
ebirs869025221
HLIrs869025221
Exacrs869025221
Varsomers869025221
Maprs869025221
PheGenIrs869025221
hapmaprs869025221
1000 genomesrs869025221
hgdprs869025221
ensemblrs869025221
gopubmedrs869025221
geneviewrs869025221
scholarrs869025221
googlers869025221
pharmgkbrs869025221
gwascentralrs869025221
openSNPrs869025221
23andMers869025221
23andMe allrs869025221
SNP Nexus

SNPshotrs869025221
SNPdbers869025221
MSV3drs869025221
GWAS Ctlgrs869025221
Max Magnitude0
ClinVar
Risk rs869025221(C;C)
Alt rs869025221(C;C)
Reference rs869025221(G;G)
Significance Probable-Pathogenic
Disease Microphthalmia
Variation info
Gene RARB
CLNDBN Microphthalmia, syndromic 12
Reversed 0
HGVS NC_000003.11:g.25635094G>C
CLNSRC
CLNACC RCV000207484.1,