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rs34595252

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs34595252(C;C)
Make rs34595252(C;T)
ReferenceGRCh38 38.1/142
Chromosome5
Position111119021
GeneWDR36
is asnp
is mentioned by
dbSNPrs34595252
ebirs34595252
HLIrs34595252
Exacrs34595252
Varsomers34595252
Maprs34595252
PheGenIrs34595252
hapmaprs34595252
1000 genomesrs34595252
hgdprs34595252
ensemblrs34595252
gopubmedrs34595252
geneviewrs34595252
scholarrs34595252
googlers34595252
pharmgkbrs34595252
gwascentralrs34595252
openSNPrs34595252
23andMers34595252
23andMe allrs34595252
SNP Nexus

SNPshotrs34595252
SNPdbers34595252
MSV3drs34595252
GWAS Ctlgrs34595252
GMAF0.001837
Max Magnitude0
OMIM609669
Desc
Variant0001
Relatedalso


ClinVar
Risk rs34595252(C;C)
Alt rs34595252(C;C)
Reference rs34595252(T;T)
Significance Pathogenic
Disease Glaucoma 1
Variation info
Gene WDR36
CLNDBN Glaucoma 1, open angle, G
Reversed 1
HGVS NC_000005.9:g.110454719A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000001647.4,