Have questions? Visit https://www.reddit.com/r/SNPedia

rs267607177

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607177(C;T)
Make rs267607177(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position36083099
GeneWDR62
is asnp
is mentioned by
dbSNPrs267607177
ebirs267607177
HLIrs267607177
Exacrs267607177
Varsomers267607177
Maprs267607177
PheGenIrs267607177
hapmaprs267607177
1000 genomesrs267607177
hgdprs267607177
ensemblrs267607177
gopubmedrs267607177
geneviewrs267607177
scholarrs267607177
googlers267607177
pharmgkbrs267607177
gwascentralrs267607177
openSNPrs267607177
23andMers267607177
23andMe allrs267607177
SNP Nexus

SNPshotrs267607177
SNPdbers267607177
MSV3drs267607177
GWAS Ctlgrs267607177
Max Magnitude0
ClinVar
Risk rs267607177(T;T)
Alt rs267607177(T;T)
Reference rs267607177(C;C)
Significance Pathogenic
Disease Primary autosomal recessive microcephaly 2
Variation info
Gene WDR62
CLNDBN Primary autosomal recessive microcephaly 2
Reversed 0
HGVS NC_000019.9:g.36574001C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000060.3,