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rs35703638

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs35703638(C;T)
Make rs35703638(T;T)
ReferenceGRCh38 38.1/142
Chromosome5
Position111106140
GeneWDR36
is asnp
is mentioned by
dbSNPrs35703638
ebirs35703638
HLIrs35703638
Exacrs35703638
Varsomers35703638
Maprs35703638
PheGenIrs35703638
hapmaprs35703638
1000 genomesrs35703638
hgdprs35703638
ensemblrs35703638
gopubmedrs35703638
geneviewrs35703638
scholarrs35703638
googlers35703638
pharmgkbrs35703638
gwascentralrs35703638
openSNPrs35703638
23andMers35703638
23andMe allrs35703638
SNP Nexus

SNPshotrs35703638
SNPdbers35703638
MSV3drs35703638
GWAS Ctlgrs35703638
GMAF0.002755
Max Magnitude0
OMIM609669
Desc
Variant0003
Relatedalso


ClinVar
Risk rs35703638(T;T)
Alt rs35703638(T;T)
Reference rs35703638(C;C)
Significance Pathogenic
Disease Glaucoma 1
Variation info
Gene WDR36
CLNDBN Glaucoma 1, open angle, G
Reversed 1
HGVS NC_000005.9:g.110441839G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001649.3,



GET Evidence
WDR36-A449T
aa_change Ala449Thr
aa_change_short A449T
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.00371885
summary