Have questions? Visit https://www.reddit.com/r/SNPedia

rs878853284

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853284(G;T)
Make rs878853284(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position3225373
GeneTUBB2B
is asnp
is mentioned by
dbSNPrs878853284
ebirs878853284
HLIrs878853284
Exacrs878853284
Varsomers878853284
Maprs878853284
PheGenIrs878853284
hapmaprs878853284
1000 genomesrs878853284
hgdprs878853284
ensemblrs878853284
gopubmedrs878853284
geneviewrs878853284
scholarrs878853284
googlers878853284
pharmgkbrs878853284
gwascentralrs878853284
openSNPrs878853284
23andMers878853284
23andMe allrs878853284
SNP Nexus

SNPshotrs878853284
SNPdbers878853284
MSV3drs878853284
GWAS Ctlgrs878853284
Max Magnitude0
ClinVar
Risk rs878853284(T;T)
Alt rs878853284(T;T)
Reference rs878853284(G;G)
Significance Pathogenic
Disease Polymicrogyria
Variation info
Gene TUBB2B
CLNDBN Polymicrogyria, asymmetric
Reversed 1
HGVS NC_000006.11:g.3225607C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000225257.1,