Rs118204022

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Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs118204022(A;G)
Make rs118204022(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position111104342
GeneWDR36
is asnp
is mentioned by
dbSNPrs118204022
Exacrs118204022
PheGenIrs118204022
nextbiors118204022
hapmaprs118204022
1000 genomesrs118204022
hgdprs118204022
ensemblrs118204022
gopubmedrs118204022
geneviewrs118204022
scholarrs118204022
googlers118204022
pharmgkbrs118204022
gwascentralrs118204022
openSNPrs118204022
23andMers118204022
23andMe allrs118204022
SNP Nexus

SNPshotrs118204022
SNPdbers118204022
MSV3drs118204022
Max Magnitude0
OMIM609669
Desc
Variant0002
Relatedalso
ClinVar
Risk rs118204022(G;G)
Alt rs118204022(G;G)
Reference rs118204022(A;A)
Significance Pathogenic
Disease Glaucoma 1
Variation info
Gene WDR36
CLNDBN Glaucoma 1, open angle, G
Reversed 0
HGVS NC_000005.9:g.110440041A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000001648.1,