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rs267607176

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607176(C;C)
Make rs267607176(C;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position36067415
GeneWDR62
is asnp
is mentioned by
dbSNPrs267607176
ebirs267607176
HLIrs267607176
Exacrs267607176
Varsomers267607176
Maprs267607176
PheGenIrs267607176
hapmaprs267607176
1000 genomesrs267607176
hgdprs267607176
ensemblrs267607176
gopubmedrs267607176
geneviewrs267607176
scholarrs267607176
googlers267607176
pharmgkbrs267607176
gwascentralrs267607176
openSNPrs267607176
23andMers267607176
23andMe allrs267607176
SNP Nexus

SNPshotrs267607176
SNPdbers267607176
MSV3drs267607176
GWAS Ctlgrs267607176
Max Magnitude0
ClinVar
Risk rs267607176(C;C)
Alt rs267607176(C;C)
Reference rs267607176(G;G)
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.36558317G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000000059.4,