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rs267607175

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607175(A;A)
Make rs267607175(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position19933469
GeneWDR35
is asnp
is mentioned by
dbSNPrs267607175
ebirs267607175
HLIrs267607175
Exacrs267607175
Varsomers267607175
Maprs267607175
PheGenIrs267607175
hapmaprs267607175
1000 genomesrs267607175
hgdprs267607175
ensemblrs267607175
gopubmedrs267607175
geneviewrs267607175
scholarrs267607175
googlers267607175
pharmgkbrs267607175
gwascentralrs267607175
openSNPrs267607175
23andMers267607175
23andMe allrs267607175
SNP Nexus

SNPshotrs267607175
SNPdbers267607175
MSV3drs267607175
GWAS Ctlgrs267607175
Max Magnitude0
ClinVar
Risk rs267607175(A;A)
Alt rs267607175(A;A)
Reference rs267607175(G;G)
Significance Pathogenic
Disease Cranioectodermal dysplasia 2
Variation info
Gene WDR35
CLNDBN Cranioectodermal dysplasia 2
Reversed 1
HGVS NC_000002.11:g.20133230C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000040.4,