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rs1057517784

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517784(A;A)
Make rs1057517784(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position31793562
GenePAX6
is asnp
is mentioned by
dbSNPrs1057517784
dbSNP (old)rs1057517784
ClinGenrs1057517784
ebirs1057517784
HLIrs1057517784
Exacrs1057517784
Gnomadrs1057517784
Varsomers1057517784
Maprs1057517784
PheGenIrs1057517784
Biobankrs1057517784
1000 genomesrs1057517784
hgdprs1057517784
ensemblrs1057517784
gopubmedrs1057517784
geneviewrs1057517784
scholarrs1057517784
googlers1057517784
pharmgkbrs1057517784
gwascentralrs1057517784
openSNPrs1057517784
23andMers1057517784
23andMe allrs1057517784
SNPshotrs1057517784
SNPdbers1057517784
MSV3drs1057517784
GWAS Ctlgrs1057517784
Max Magnitude0
ClinVar
Risk rs1057517784(A;A)
Alt rs1057517784(A;A)
Reference Rs1057517784(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PAX6
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.31815110A>T
CLNSRC
CLNACC RCV000413082.1,