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rs1057517783

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517783(C;C)
Make rs1057517783(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position31793651
GenePAX6
is asnp
is mentioned by
dbSNPrs1057517783
dbSNP (old)rs1057517783
ClinGenrs1057517783
ebirs1057517783
HLIrs1057517783
Exacrs1057517783
Gnomadrs1057517783
Varsomers1057517783
Maprs1057517783
PheGenIrs1057517783
Biobankrs1057517783
1000 genomesrs1057517783
hgdprs1057517783
ensemblrs1057517783
gopubmedrs1057517783
geneviewrs1057517783
scholarrs1057517783
googlers1057517783
pharmgkbrs1057517783
gwascentralrs1057517783
openSNPrs1057517783
23andMers1057517783
23andMe allrs1057517783
SNPshotrs1057517783
SNPdbers1057517783
MSV3drs1057517783
GWAS Ctlgrs1057517783
Max Magnitude0
ClinVar
Risk rs1057517783(C;C)
Alt rs1057517783(C;C)
Reference Rs1057517783(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PAX6
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.31815199C>G
CLNSRC
CLNACC RCV000414749.1,