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rs397515334

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515334(-;-)
Make rs397515334(-;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position19931375
GeneWDR35
is asnp
is mentioned by
dbSNPrs397515334
ebirs397515334
HLIrs397515334
Exacrs397515334
Varsomers397515334
Maprs397515334
PheGenIrs397515334
hapmaprs397515334
1000 genomesrs397515334
hgdprs397515334
ensemblrs397515334
gopubmedrs397515334
geneviewrs397515334
scholarrs397515334
googlers397515334
pharmgkbrs397515334
gwascentralrs397515334
openSNPrs397515334
23andMers397515334
23andMe allrs397515334
SNP Nexus

SNPshotrs397515334
SNPdbers397515334
MSV3drs397515334
GWAS Ctlgrs397515334
Max Magnitude0
ClinVar
Risk rs397515334(;)
Alt rs397515334(;)
Reference rs397515334(C;C)
Significance Pathogenic
Disease Cranioectodermal dysplasia 2
Variation info
Gene WDR35
CLNDBN Cranioectodermal dysplasia 2
Reversed 1
HGVS NC_000002.11:g.20131136delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000000039.5,