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rs587776899

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776899(-;-)
Make rs587776899(-;T)
Make rs587776899(T;T)
ReferenceGRCh38 38.1/142
Chromosome19
Position36104605
GeneWDR62
is asnp
is mentioned by
dbSNPrs587776899
ebirs587776899
HLIrs587776899
Exacrs587776899
Varsomers587776899
Maprs587776899
PheGenIrs587776899
hapmaprs587776899
1000 genomesrs587776899
hgdprs587776899
ensemblrs587776899
gopubmedrs587776899
geneviewrs587776899
scholarrs587776899
googlers587776899
pharmgkbrs587776899
gwascentralrs587776899
openSNPrs587776899
23andMers587776899
23andMe allrs587776899
SNP Nexus

SNPshotrs587776899
SNPdbers587776899
MSV3drs587776899
GWAS Ctlgrs587776899
Max Magnitude0
ClinVar
Risk rs587776899(T;T)
Alt rs587776899(T;T)
Reference rs587776899(;)
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.36595507dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000024030.4,