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rs104886474

From SNPedia

Orientationminus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104886474(C;C)
Make rs104886474(C;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position151181424
GeneASB10
is asnp
is mentioned by
dbSNPrs104886474
ebirs104886474
HLIrs104886474
Exacrs104886474
Varsomers104886474
Maprs104886474
PheGenIrs104886474
hapmaprs104886474
1000 genomesrs104886474
hgdprs104886474
ensemblrs104886474
gopubmedrs104886474
geneviewrs104886474
scholarrs104886474
googlers104886474
pharmgkbrs104886474
gwascentralrs104886474
openSNPrs104886474
23andMers104886474
23andMe allrs104886474
SNP Nexus

SNPshotrs104886474
SNPdbers104886474
MSV3drs104886474
GWAS Ctlgrs104886474
GMAF0.0009183
Max Magnitude0
ClinVar
Risk rs104886474(C;C)
Alt rs104886474(C;C)
Reference rs104886474(G;G)
Significance Pathogenic
Disease Glaucoma 1
Variation info
Gene ASB10
CLNDBN Glaucoma 1, open angle, F
Reversed 1
HGVS NC_000007.13:g.150878511C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000043658.3,


[PMID 10037570] GLC1F, a new primary open-angle glaucoma locus, maps to 7q35-q36.