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rs794726661

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794726661(A;G)
Make rs794726661(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position31790862
GenePAX6
is asnp
is mentioned by
dbSNPrs794726661
ebirs794726661
HLIrs794726661
Exacrs794726661
Varsomers794726661
Maprs794726661
PheGenIrs794726661
hapmaprs794726661
1000 genomesrs794726661
hgdprs794726661
ensemblrs794726661
gopubmedrs794726661
geneviewrs794726661
scholarrs794726661
googlers794726661
pharmgkbrs794726661
gwascentralrs794726661
openSNPrs794726661
23andMers794726661
23andMe allrs794726661
SNP Nexus

SNPshotrs794726661
SNPdbers794726661
MSV3drs794726661
GWAS Ctlgrs794726661
Max Magnitude0
ClinVar
Risk rs794726661(G;G)
Alt rs794726661(G;G)
Reference rs794726661(A;A)
Significance Pathogenic
Disease Congenital aniridia
Variation info
Gene PAX6
CLNDBN Congenital aniridia
Reversed 1
HGVS NC_000011.9:g.31812410T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000003633.4,