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rs587776900

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776900(-;-)
Make rs587776900(-;C)
Make rs587776900(C;C)
ReferenceGRCh38 38.1/142
Chromosome19
Position36103764
GeneWDR62
is asnp
is mentioned by
dbSNPrs587776900
ebirs587776900
HLIrs587776900
Exacrs587776900
Varsomers587776900
Maprs587776900
PheGenIrs587776900
hapmaprs587776900
1000 genomesrs587776900
hgdprs587776900
ensemblrs587776900
gopubmedrs587776900
geneviewrs587776900
scholarrs587776900
googlers587776900
pharmgkbrs587776900
gwascentralrs587776900
openSNPrs587776900
23andMers587776900
23andMe allrs587776900
SNP Nexus

SNPshotrs587776900
SNPdbers587776900
MSV3drs587776900
GWAS Ctlgrs587776900
Max Magnitude0
ClinVar
Risk rs587776900(C;C)
Alt rs587776900(C;C)
Reference rs587776900(;)
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.36594666dupC
CLNSRC OMIM Allelic Variant
CLNACC RCV000024032.5,