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rs1057520755

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520755(A;A)
Make rs1057520755(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position31800728
GenePAX6
is asnp
is mentioned by
dbSNPrs1057520755
dbSNP (old)rs1057520755
ClinGenrs1057520755
ebirs1057520755
HLIrs1057520755
Exacrs1057520755
Gnomadrs1057520755
Varsomers1057520755
Maprs1057520755
PheGenIrs1057520755
Biobankrs1057520755
1000 genomesrs1057520755
hgdprs1057520755
ensemblrs1057520755
gopubmedrs1057520755
geneviewrs1057520755
scholarrs1057520755
googlers1057520755
pharmgkbrs1057520755
gwascentralrs1057520755
openSNPrs1057520755
23andMers1057520755
23andMe allrs1057520755
SNPshotrs1057520755
SNPdbers1057520755
MSV3drs1057520755
GWAS Ctlgrs1057520755
Max Magnitude0
ClinVar
Risk rs1057520755(A;A)
Alt rs1057520755(A;A)
Reference Rs1057520755(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PAX6
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.31822276C>T
CLNSRC
CLNACC RCV000419144.1,