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rs587784554

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587784554(A;G)
Make rs587784554(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position36102854
GeneWDR62
is asnp
is mentioned by
dbSNPrs587784554
ebirs587784554
HLIrs587784554
Exacrs587784554
Varsomers587784554
Maprs587784554
PheGenIrs587784554
hapmaprs587784554
1000 genomesrs587784554
hgdprs587784554
ensemblrs587784554
gopubmedrs587784554
geneviewrs587784554
scholarrs587784554
googlers587784554
pharmgkbrs587784554
gwascentralrs587784554
openSNPrs587784554
23andMers587784554
23andMe allrs587784554
SNP Nexus

SNPshotrs587784554
SNPdbers587784554
MSV3drs587784554
GWAS Ctlgrs587784554
Max Magnitude0
ClinVar
Risk rs587784554(G;G)
Alt rs587784554(G;G)
Reference rs587784554(A;A)
Significance Probable-Pathogenic
Disease Primary autosomal recessive microcephaly 2
Variation info
Gene WDR62
CLNDBN Primary autosomal recessive microcephaly 2
Reversed 0
HGVS NC_000019.9:g.36593756A>G
CLNSRC
CLNACC RCV000147953.1,