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rs1057517781

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057517781(-;G)
Make rs1057517781(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position31802735
GenePAX6
is asnp
is mentioned by
dbSNPrs1057517781
dbSNP (old)rs1057517781
ClinGenrs1057517781
ebirs1057517781
HLIrs1057517781
Exacrs1057517781
Gnomadrs1057517781
Varsomers1057517781
Maprs1057517781
PheGenIrs1057517781
Biobankrs1057517781
1000 genomesrs1057517781
hgdprs1057517781
ensemblrs1057517781
gopubmedrs1057517781
geneviewrs1057517781
scholarrs1057517781
googlers1057517781
pharmgkbrs1057517781
gwascentralrs1057517781
openSNPrs1057517781
23andMers1057517781
23andMe allrs1057517781
SNPshotrs1057517781
SNPdbers1057517781
MSV3drs1057517781
GWAS Ctlgrs1057517781
Max Magnitude0
ClinVar
Risk rs1057517781(G;G)
Alt rs1057517781(G;G)
Reference Rs1057517781(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene PAX6
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.31824284dupC
CLNSRC
CLNACC RCV000413008.1,