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rs116529882

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs116529882(A;A)
Make rs116529882(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position111110280
GeneWDR36
is asnp
is mentioned by
dbSNPrs116529882
dbSNP (classic)rs116529882
ClinGenrs116529882
ebirs116529882
HLIrs116529882
Exacrs116529882
Gnomadrs116529882
Varsomers116529882
LitVarrs116529882
Maprs116529882
PheGenIrs116529882
Biobankrs116529882
1000 genomesrs116529882
hgdprs116529882
ensemblrs116529882
geneviewrs116529882
scholarrs116529882
googlers116529882
pharmgkbrs116529882
gwascentralrs116529882
openSNPrs116529882
23andMers116529882
SNPshotrs116529882
SNPdbers116529882
MSV3drs116529882
GWAS Ctlgrs116529882
GMAF0.0004591
Max Magnitude0
OMIM609669
Desc
Variant0004
Relatedalso
ClinVar
Risk rs116529882(A;A)
Alt rs116529882(A;A)
Reference Rs116529882(G;G)
Significance Pathogenic
Disease Glaucoma 1 Primary open angle glaucoma
Variation info
Gene WDR36
CLNDBN Glaucoma 1, open angle, G Primary open angle glaucoma
Reversed 0
HGVS NC_000005.9:g.110445979G>A
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000001650.3, RCV000267516.1,