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rs397515536

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397515536(A;A)
Make rs397515536(A;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position19975596
GeneWDR35
is asnp
is mentioned by
dbSNPrs397515536
ebirs397515536
HLIrs397515536
Exacrs397515536
Varsomers397515536
Maprs397515536
PheGenIrs397515536
hapmaprs397515536
1000 genomesrs397515536
hgdprs397515536
ensemblrs397515536
gopubmedrs397515536
geneviewrs397515536
scholarrs397515536
googlers397515536
pharmgkbrs397515536
gwascentralrs397515536
openSNPrs397515536
23andMers397515536
23andMe allrs397515536
SNP Nexus

SNPshotrs397515536
SNPdbers397515536
MSV3drs397515536
GWAS Ctlgrs397515536
Max Magnitude0
ClinVar
Risk rs397515536(A;A)
Alt rs397515536(A;A)
Reference rs397515536(T;T)
Significance Pathogenic
Disease Cranioectodermal dysplasia 2
Variation info
Gene WDR35
CLNDBN Cranioectodermal dysplasia 2
Reversed 1
HGVS NC_000002.11:g.20175357A>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000055835.1,