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rs878853162

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853162(C;T)
Make rs878853162(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position30723724
GeneTUBB
is asnp
is mentioned by
dbSNPrs878853162
ebirs878853162
HLIrs878853162
Exacrs878853162
Varsomers878853162
Maprs878853162
PheGenIrs878853162
hapmaprs878853162
1000 genomesrs878853162
hgdprs878853162
ensemblrs878853162
gopubmedrs878853162
geneviewrs878853162
scholarrs878853162
googlers878853162
pharmgkbrs878853162
gwascentralrs878853162
openSNPrs878853162
23andMers878853162
23andMe allrs878853162
SNP Nexus

SNPshotrs878853162
SNPdbers878853162
MSV3drs878853162
GWAS Ctlgrs878853162
Max Magnitude0
ClinVar
Risk rs878853162(T;T)
Alt rs878853162(T;T)
Reference rs878853162(C;C)
Significance Pathogenic
Disease Cortical dysplasia
Variation info
Gene TUBB
CLNDBN Cortical dysplasia, complex, with other brain malformations 6
Reversed 0
HGVS NC_000006.11:g.30691501C>T
CLNSRC
CLNACC RCV000224973.1,