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rs1057517782

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517782(G;G)
Make rs1057517782(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position31802702
GenePAX6
is asnp
is mentioned by
dbSNPrs1057517782
dbSNP (old)rs1057517782
ClinGenrs1057517782
ebirs1057517782
HLIrs1057517782
Exacrs1057517782
Gnomadrs1057517782
Varsomers1057517782
Maprs1057517782
PheGenIrs1057517782
Biobankrs1057517782
1000 genomesrs1057517782
hgdprs1057517782
ensemblrs1057517782
gopubmedrs1057517782
geneviewrs1057517782
scholarrs1057517782
googlers1057517782
pharmgkbrs1057517782
gwascentralrs1057517782
openSNPrs1057517782
23andMers1057517782
23andMe allrs1057517782
SNPshotrs1057517782
SNPdbers1057517782
MSV3drs1057517782
GWAS Ctlgrs1057517782
Max Magnitude0
ClinVar
Risk rs1057517782(G;G)
Alt rs1057517782(G;G)
Reference Rs1057517782(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene PAX6
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.31824250A>C
CLNSRC
CLNACC RCV000413692.1,