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rs398123296

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123296(-;-)
Make rs398123296(-;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position31802799
GenePAX6
is asnp
is mentioned by
dbSNPrs398123296
ebirs398123296
HLIrs398123296
Exacrs398123296
Varsomers398123296
Maprs398123296
PheGenIrs398123296
hapmaprs398123296
1000 genomesrs398123296
hgdprs398123296
ensemblrs398123296
gopubmedrs398123296
geneviewrs398123296
scholarrs398123296
googlers398123296
pharmgkbrs398123296
gwascentralrs398123296
openSNPrs398123296
23andMers398123296
23andMe allrs398123296
SNP Nexus

SNPshotrs398123296
SNPdbers398123296
MSV3drs398123296
GWAS Ctlgrs398123296
Max Magnitude0
ClinVar
Risk rs398123296(;)
Alt rs398123296(;)
Reference rs398123296(G;G)
Significance Pathogenic
Disease not provided Congenital aniridia
Variation info
Gene PAX6
CLNDBN not provided Congenital aniridia
Reversed 1
HGVS NC_000011.9:g.31824347delC
CLNSRC ClinVar
CLNACC RCV000078544.3, RCV000178745.1,