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rs75654767

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs75654767(A;A)
Make rs75654767(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position13136766
GeneOPTN
is asnp
is mentioned by
dbSNPrs75654767
ebirs75654767
HLIrs75654767
Exacrs75654767
Varsomers75654767
Maprs75654767
PheGenIrs75654767
hapmaprs75654767
1000 genomesrs75654767
hgdprs75654767
ensemblrs75654767
gopubmedrs75654767
geneviewrs75654767
scholarrs75654767
googlers75654767
pharmgkbrs75654767
gwascentralrs75654767
openSNPrs75654767
23andMers75654767
23andMe allrs75654767
SNP Nexus

SNPshotrs75654767
SNPdbers75654767
MSV3drs75654767
GWAS Ctlgrs75654767
Merged fromRs28939689
GMAF0.0101
Max Magnitude0
OMIM602432
Desc
Variant0003
Relatedalso
ClinVar
Risk rs75654767(A;A)
Alt rs75654767(A;A)
Reference rs75654767(G;G)
Significance Pathogenic
Disease Glaucoma 1
Variation info
Gene OPTN
CLNDBN Glaucoma 1, open angle, e
Reversed 0
HGVS NC_000010.10:g.13178766G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007515.2,