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rs397515535

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397515535(A;G)
Make rs397515535(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position19931354
GeneWDR35
is asnp
is mentioned by
dbSNPrs397515535
ebirs397515535
HLIrs397515535
Exacrs397515535
Varsomers397515535
Maprs397515535
PheGenIrs397515535
hapmaprs397515535
1000 genomesrs397515535
hgdprs397515535
ensemblrs397515535
gopubmedrs397515535
geneviewrs397515535
scholarrs397515535
googlers397515535
pharmgkbrs397515535
gwascentralrs397515535
openSNPrs397515535
23andMers397515535
23andMe allrs397515535
SNP Nexus

SNPshotrs397515535
SNPdbers397515535
MSV3drs397515535
GWAS Ctlgrs397515535
Max Magnitude0
ClinVar
Risk rs397515535(G;G)
Alt rs397515535(G;G)
Reference rs397515535(A;A)
Significance Pathogenic
Disease Cranioectodermal dysplasia 2
Variation info
Gene WDR35
CLNDBN Cranioectodermal dysplasia 2
Reversed 1
HGVS NC_000002.11:g.20131115T>C
CLNSRC ClinVar GeneReviews
CLNACC RCV000055834.1,