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rs587784543

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587784543(A;A)
Make rs587784543(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position36083171
GeneWDR62
is asnp
is mentioned by
dbSNPrs587784543
ebirs587784543
HLIrs587784543
Exacrs587784543
Varsomers587784543
Maprs587784543
PheGenIrs587784543
hapmaprs587784543
1000 genomesrs587784543
hgdprs587784543
ensemblrs587784543
gopubmedrs587784543
geneviewrs587784543
scholarrs587784543
googlers587784543
pharmgkbrs587784543
gwascentralrs587784543
openSNPrs587784543
23andMers587784543
23andMe allrs587784543
SNP Nexus

SNPshotrs587784543
SNPdbers587784543
MSV3drs587784543
GWAS Ctlgrs587784543
Max Magnitude0
ClinVar
Risk rs587784543(A;A)
Alt rs587784543(A;A)
Reference rs587784543(G;G)
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.36574073G>A
CLNSRC
CLNACC RCV000147915.1,