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rs587776901

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587776901(-;-)
Make rs587776901(-;T)
ReferenceGRCh38 38.1/142
Chromosome19
Position36065988
GeneWDR62
is asnp
is mentioned by
dbSNPrs587776901
ebirs587776901
HLIrs587776901
Exacrs587776901
Varsomers587776901
Maprs587776901
PheGenIrs587776901
hapmaprs587776901
1000 genomesrs587776901
hgdprs587776901
ensemblrs587776901
gopubmedrs587776901
geneviewrs587776901
scholarrs587776901
googlers587776901
pharmgkbrs587776901
gwascentralrs587776901
openSNPrs587776901
23andMers587776901
23andMe allrs587776901
SNP Nexus

SNPshotrs587776901
SNPdbers587776901
MSV3drs587776901
GWAS Ctlgrs587776901
Max Magnitude0
ClinVar
Risk rs587776901(;)
Alt rs587776901(;)
Reference rs587776901(T;T)
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.36556890delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000024033.4,