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rs864309686

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs864309686(A;A)
Make rs864309686(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position31801721
GenePAX6
is asnp
is mentioned by
dbSNPrs864309686
ebirs864309686
HLIrs864309686
Exacrs864309686
Varsomers864309686
Maprs864309686
PheGenIrs864309686
hapmaprs864309686
1000 genomesrs864309686
hgdprs864309686
ensemblrs864309686
gopubmedrs864309686
geneviewrs864309686
scholarrs864309686
googlers864309686
pharmgkbrs864309686
gwascentralrs864309686
openSNPrs864309686
23andMers864309686
23andMe allrs864309686
SNP Nexus

SNPshotrs864309686
SNPdbers864309686
MSV3drs864309686
GWAS Ctlgrs864309686
Max Magnitude0
ClinVar
Risk rs864309686(A;A)
Alt rs864309686(A;A)
Reference rs864309686(T;T)
Significance Probable-Pathogenic
Disease Congenital cataract
Variation info
Gene PAX6
CLNDBN Congenital cataract
Reversed 1
HGVS NC_000011.9:g.31823269A>T
CLNSRC
CLNACC RCV000203333.1,