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rs878852979

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878852979(A;A)
Make rs878852979(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position31810826
GenePAX6
is asnp
is mentioned by
dbSNPrs878852979
ebirs878852979
HLIrs878852979
Exacrs878852979
Varsomers878852979
Maprs878852979
PheGenIrs878852979
hapmaprs878852979
1000 genomesrs878852979
hgdprs878852979
ensemblrs878852979
gopubmedrs878852979
geneviewrs878852979
scholarrs878852979
googlers878852979
pharmgkbrs878852979
gwascentralrs878852979
openSNPrs878852979
23andMers878852979
23andMe allrs878852979
SNP Nexus

SNPshotrs878852979
SNPdbers878852979
MSV3drs878852979
GWAS Ctlgrs878852979
Max Magnitude0
ClinVar
Risk rs878852979(A;A)
Alt rs878852979(A;A)
Reference rs878852979(T;T)
Significance Pathogenic
Disease Congenital aniridia
Variation info
Gene PAX6
CLNDBN Congenital aniridia
Reversed 1
HGVS NC_000011.9:g.31832374A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003651.3,