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rs387907084

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387907084(A;A)
Make rs387907084(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position36058795
GeneWDR62
is asnp
is mentioned by
dbSNPrs387907084
ebirs387907084
HLIrs387907084
Exacrs387907084
Varsomers387907084
Maprs387907084
PheGenIrs387907084
hapmaprs387907084
1000 genomesrs387907084
hgdprs387907084
ensemblrs387907084
gopubmedrs387907084
geneviewrs387907084
scholarrs387907084
googlers387907084
pharmgkbrs387907084
gwascentralrs387907084
openSNPrs387907084
23andMers387907084
23andMe allrs387907084
SNP Nexus

SNPshotrs387907084
SNPdbers387907084
MSV3drs387907084
GWAS Ctlgrs387907084
Max Magnitude0
ClinVar
Risk rs387907084(A;A)
Alt rs387907084(A;A)
Reference rs387907084(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.36549697G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000024034.4,