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rs1057517785

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517785(C;T)
Make rs1057517785(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position31793521
GenePAX6
is asnp
is mentioned by
dbSNPrs1057517785
dbSNP (old)rs1057517785
ClinGenrs1057517785
ebirs1057517785
HLIrs1057517785
Exacrs1057517785
Gnomadrs1057517785
Varsomers1057517785
Maprs1057517785
PheGenIrs1057517785
Biobankrs1057517785
1000 genomesrs1057517785
hgdprs1057517785
ensemblrs1057517785
gopubmedrs1057517785
geneviewrs1057517785
scholarrs1057517785
googlers1057517785
pharmgkbrs1057517785
gwascentralrs1057517785
openSNPrs1057517785
23andMers1057517785
23andMe allrs1057517785
SNPshotrs1057517785
SNPdbers1057517785
MSV3drs1057517785
GWAS Ctlgrs1057517785
Max Magnitude0
ClinVar
Risk rs1057517785(T;T)
Alt rs1057517785(T;T)
Reference Rs1057517785(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PAX6
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.31815069G>A
CLNSRC
CLNACC RCV000413962.1,