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rs1057517780

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517780(-;-)
Make rs1057517780(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position31802736
GenePAX6
is asnp
is mentioned by
dbSNPrs1057517780
dbSNP (old)rs1057517780
ClinGenrs1057517780
ebirs1057517780
HLIrs1057517780
Exacrs1057517780
Gnomadrs1057517780
Varsomers1057517780
Maprs1057517780
PheGenIrs1057517780
Biobankrs1057517780
1000 genomesrs1057517780
hgdprs1057517780
ensemblrs1057517780
gopubmedrs1057517780
geneviewrs1057517780
scholarrs1057517780
googlers1057517780
pharmgkbrs1057517780
gwascentralrs1057517780
openSNPrs1057517780
23andMers1057517780
23andMe allrs1057517780
SNPshotrs1057517780
SNPdbers1057517780
MSV3drs1057517780
GWAS Ctlgrs1057517780
Max Magnitude0
ClinVar
Risk rs1057517780(-;-)
Alt rs1057517780(-;-)
Reference Rs1057517780(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PAX6
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.31824284delC
CLNSRC
CLNACC RCV000414410.1,