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rs587784553

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587784553(A;A)
Make rs587784553(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position36060031
GeneWDR62
is asnp
is mentioned by
dbSNPrs587784553
ebirs587784553
HLIrs587784553
Exacrs587784553
Varsomers587784553
Maprs587784553
PheGenIrs587784553
hapmaprs587784553
1000 genomesrs587784553
hgdprs587784553
ensemblrs587784553
gopubmedrs587784553
geneviewrs587784553
scholarrs587784553
googlers587784553
pharmgkbrs587784553
gwascentralrs587784553
openSNPrs587784553
23andMers587784553
23andMe allrs587784553
SNP Nexus

SNPshotrs587784553
SNPdbers587784553
MSV3drs587784553
GWAS Ctlgrs587784553
Max Magnitude0
ClinVar
Risk rs587784553(A;A)
Alt rs587784553(A;A)
Reference rs587784553(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.36550933G>A
CLNSRC
CLNACC RCV000147952.1,