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rs587784549

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587784549(C;G)
Make rs587784549(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position36099533
GeneWDR62
is asnp
is mentioned by
dbSNPrs587784549
ebirs587784549
HLIrs587784549
Exacrs587784549
Varsomers587784549
Maprs587784549
PheGenIrs587784549
hapmaprs587784549
1000 genomesrs587784549
hgdprs587784549
ensemblrs587784549
gopubmedrs587784549
geneviewrs587784549
scholarrs587784549
googlers587784549
pharmgkbrs587784549
gwascentralrs587784549
openSNPrs587784549
23andMers587784549
23andMe allrs587784549
SNP Nexus

SNPshotrs587784549
SNPdbers587784549
MSV3drs587784549
GWAS Ctlgrs587784549
Max Magnitude0
ClinVar
Risk rs587784549(G;G)
Alt rs587784549(G;G)
Reference rs587784549(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.36590435C>G
CLNSRC
CLNACC RCV000147941.1,