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rs397515533

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397515533(C;C)
Make rs397515533(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position19946536
GeneWDR35
is asnp
is mentioned by
dbSNPrs397515533
ebirs397515533
HLIrs397515533
Exacrs397515533
Varsomers397515533
Maprs397515533
PheGenIrs397515533
hapmaprs397515533
1000 genomesrs397515533
hgdprs397515533
ensemblrs397515533
gopubmedrs397515533
geneviewrs397515533
scholarrs397515533
googlers397515533
pharmgkbrs397515533
gwascentralrs397515533
openSNPrs397515533
23andMers397515533
23andMe allrs397515533
SNP Nexus

SNPshotrs397515533
SNPdbers397515533
MSV3drs397515533
GWAS Ctlgrs397515533
Max Magnitude0
ClinVar
Risk rs397515533(C;C)
Alt rs397515533(C;C)
Reference rs397515533(T;T)
Significance Pathogenic
Disease Cranioectodermal dysplasia 2
Variation info
Gene WDR35
CLNDBN Cranioectodermal dysplasia 2
Reversed 1
HGVS NC_000002.11:g.20146297A>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000055831.1,