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rs1064795810

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome14
Position56804250
GeneOTX2
is asnp
is mentioned by
dbSNPrs1064795810
dbSNP (classic)rs1064795810
ClinGenrs1064795810
ebirs1064795810
HLIrs1064795810
Exacrs1064795810
Gnomadrs1064795810
Varsomers1064795810
LitVarrs1064795810
Maprs1064795810
PheGenIrs1064795810
Biobankrs1064795810
1000 genomesrs1064795810
hgdprs1064795810
ensemblrs1064795810
geneviewrs1064795810
scholarrs1064795810
googlers1064795810
pharmgkbrs1064795810
gwascentralrs1064795810
openSNPrs1064795810
23andMers1064795810
23andMe allrs1064795810
SNPshotrs1064795810
SNPdbers1064795810
MSV3drs1064795810
GWAS Ctlgrs1064795810
Max Magnitude0
ClinVar
Risk rs1064795810(A;A)
Alt rs1064795810(A;A)
Reference Rs1064795810(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene OTX2
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.57270968G>T
CLNSRC
CLNACC RCV000480483.1,