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rs104886488

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104886488(A;A)
Make rs104886488(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position151186916
GeneASB10
is asnp
is mentioned by
dbSNPrs104886488
ebirs104886488
HLIrs104886488
Exacrs104886488
Varsomers104886488
Maprs104886488
PheGenIrs104886488
hapmaprs104886488
1000 genomesrs104886488
hgdprs104886488
ensemblrs104886488
gopubmedrs104886488
geneviewrs104886488
scholarrs104886488
googlers104886488
pharmgkbrs104886488
gwascentralrs104886488
openSNPrs104886488
23andMers104886488
23andMe allrs104886488
SNP Nexus

SNPshotrs104886488
SNPdbers104886488
MSV3drs104886488
GWAS Ctlgrs104886488
GMAF0.001377
Max Magnitude0
ClinVar
Risk rs104886488(A;A)
Alt rs104886488(A;A)
Reference rs104886488(G;G)
Significance Pathogenic
Disease Glaucoma 1
Variation info
Gene ASB10
CLNDBN Glaucoma 1, open angle, F
Reversed 1
HGVS NC_000007.13:g.150884003C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000043659.3,


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