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rs267607174

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607174(A;G)
Make rs267607174(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position19945787
GeneWDR35
is asnp
is mentioned by
dbSNPrs267607174
ebirs267607174
HLIrs267607174
Exacrs267607174
Varsomers267607174
Maprs267607174
PheGenIrs267607174
hapmaprs267607174
1000 genomesrs267607174
hgdprs267607174
ensemblrs267607174
gopubmedrs267607174
geneviewrs267607174
scholarrs267607174
googlers267607174
pharmgkbrs267607174
gwascentralrs267607174
openSNPrs267607174
23andMers267607174
23andMe allrs267607174
SNP Nexus

SNPshotrs267607174
SNPdbers267607174
MSV3drs267607174
GWAS Ctlgrs267607174
Max Magnitude0
ClinVar
Risk rs267607174(G;G)
Alt rs267607174(G;G)
Reference rs267607174(A;A)
Significance Pathogenic
Disease Cranioectodermal dysplasia 2
Variation info
Gene WDR35
CLNDBN Cranioectodermal dysplasia 2
Reversed 1
HGVS NC_000002.11:g.20145548T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000000038.4,