Rs116529882

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Orientationplus
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
Exacrs116529882
PheGenIrs116529882
nextbiors116529882
hapmaprs116529882
1000 genomesrs116529882
hgdprs116529882
ensemblrs116529882
gopubmedrs116529882
geneviewrs116529882
scholarrs116529882
googlers116529882
pharmgkbrs116529882
gwascentralrs116529882
openSNPrs116529882
23andMers116529882
23andMe allrs116529882
SNP Nexus

SNPshotrs116529882
SNPdbers116529882
MSV3drs116529882
GMAF0.0004591
OMIM609669
Desc
Variant0004
Relatedalso
ClinVar
Risk rs116529882(A;A)
Alt rs116529882(A;A)
Reference rs116529882(G;G)
Significance Pathogenic
Disease Glaucoma 1
Variation info
Gene WDR36
CLNDBN Glaucoma 1, open angle, G
Reversed 0
HGVS NC_000005.9:g.110445979G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001650.1,