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rs878853257

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853257(A;A)
Make rs878853257(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position89935064
GeneTUBB3
is asnp
is mentioned by
dbSNPrs878853257
ebirs878853257
HLIrs878853257
Exacrs878853257
Varsomers878853257
Maprs878853257
PheGenIrs878853257
hapmaprs878853257
1000 genomesrs878853257
hgdprs878853257
ensemblrs878853257
gopubmedrs878853257
geneviewrs878853257
scholarrs878853257
googlers878853257
pharmgkbrs878853257
gwascentralrs878853257
openSNPrs878853257
23andMers878853257
23andMe allrs878853257
SNP Nexus

SNPshotrs878853257
SNPdbers878853257
MSV3drs878853257
GWAS Ctlgrs878853257
Max Magnitude0
ClinVar
Risk rs878853257(A;A)
Alt rs878853257(A;A)
Reference rs878853257(G;G)
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.90001472G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023204.3,