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rs786205467

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205467(C;G)
Make rs786205467(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position31793492
GenePAX6
is asnp
is mentioned by
dbSNPrs786205467
ebirs786205467
HLIrs786205467
Exacrs786205467
Varsomers786205467
Maprs786205467
PheGenIrs786205467
hapmaprs786205467
1000 genomesrs786205467
hgdprs786205467
ensemblrs786205467
gopubmedrs786205467
geneviewrs786205467
scholarrs786205467
googlers786205467
pharmgkbrs786205467
gwascentralrs786205467
openSNPrs786205467
23andMers786205467
23andMe allrs786205467
SNP Nexus

SNPshotrs786205467
SNPdbers786205467
MSV3drs786205467
GWAS Ctlgrs786205467
Max Magnitude0
ClinVar
Risk rs786205467(G;G)
Alt rs786205467(G;G)
Reference rs786205467(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PAX6
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.31815040G>C
CLNSRC
CLNACC RCV000171191.1,