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rs376633424

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs376633424(C;T)
Make rs376633424(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position36102820
GeneWDR62
is asnp
is mentioned by
dbSNPrs376633424
ebirs376633424
HLIrs376633424
Exacrs376633424
Varsomers376633424
Maprs376633424
PheGenIrs376633424
hapmaprs376633424
1000 genomesrs376633424
hgdprs376633424
ensemblrs376633424
gopubmedrs376633424
geneviewrs376633424
scholarrs376633424
googlers376633424
pharmgkbrs376633424
gwascentralrs376633424
openSNPrs376633424
23andMers376633424
23andMe allrs376633424
SNP Nexus

SNPshotrs376633424
SNPdbers376633424
MSV3drs376633424
GWAS Ctlgrs376633424
Max Magnitude0
ClinVar
Risk rs376633424(T;T)
Alt rs376633424(T;T)
Reference rs376633424(C;C)
Significance Pathogenic
Disease Abnormality of neuronal migration
Variation info
Gene WDR62
CLNDBN Abnormality of neuronal migration
Reversed 0
HGVS NC_000019.9:g.36593722C>T
CLNSRC
CLNACC RCV000201333.1,