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rs878853258

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853258(C;T)
Make rs878853258(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position89935356
GeneTUBB3
is asnp
is mentioned by
dbSNPrs878853258
ebirs878853258
HLIrs878853258
Exacrs878853258
Varsomers878853258
Maprs878853258
PheGenIrs878853258
hapmaprs878853258
1000 genomesrs878853258
hgdprs878853258
ensemblrs878853258
gopubmedrs878853258
geneviewrs878853258
scholarrs878853258
googlers878853258
pharmgkbrs878853258
gwascentralrs878853258
openSNPrs878853258
23andMers878853258
23andMe allrs878853258
SNP Nexus

SNPshotrs878853258
SNPdbers878853258
MSV3drs878853258
GWAS Ctlgrs878853258
Max Magnitude0
ClinVar
Risk rs878853258(T;T)
Alt rs878853258(T;T)
Reference rs878853258(C;C)
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.90001764C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023205.3,