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rs377731205

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs377731205(C;T)
Make rs377731205(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position36097074
GeneWDR62
is asnp
is mentioned by
dbSNPrs377731205
ebirs377731205
HLIrs377731205
Exacrs377731205
Varsomers377731205
Maprs377731205
PheGenIrs377731205
hapmaprs377731205
1000 genomesrs377731205
hgdprs377731205
ensemblrs377731205
gopubmedrs377731205
geneviewrs377731205
scholarrs377731205
googlers377731205
pharmgkbrs377731205
gwascentralrs377731205
openSNPrs377731205
23andMers377731205
23andMe allrs377731205
SNP Nexus

SNPshotrs377731205
SNPdbers377731205
MSV3drs377731205
GWAS Ctlgrs377731205
Max Magnitude0
ClinVar
Risk rs377731205(T;T)
Alt rs377731205(T;T)
Reference rs377731205(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.36587976C>T
CLNSRC
CLNACC RCV000201333.1,