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rs878853256

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878853256(A;G)
Make rs878853256(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position89935418
GeneTUBB3
is asnp
is mentioned by
dbSNPrs878853256
ebirs878853256
HLIrs878853256
Exacrs878853256
Varsomers878853256
Maprs878853256
PheGenIrs878853256
hapmaprs878853256
1000 genomesrs878853256
hgdprs878853256
ensemblrs878853256
gopubmedrs878853256
geneviewrs878853256
scholarrs878853256
googlers878853256
pharmgkbrs878853256
gwascentralrs878853256
openSNPrs878853256
23andMers878853256
23andMe allrs878853256
SNP Nexus

SNPshotrs878853256
SNPdbers878853256
MSV3drs878853256
GWAS Ctlgrs878853256
Max Magnitude0
ClinVar
Risk rs878853256(G;G)
Alt rs878853256(G;G)
Reference rs878853256(A;A)
Significance Pathogenic
Disease Cortical dysplasia
Variation info
Gene TUBB3
CLNDBN Cortical dysplasia, complex, with other brain malformations 1
Reversed 0
HGVS NC_000016.9:g.90001826A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000023202.3,