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rs587777357

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777357(A;A)
Make rs587777357(A;G)
ReferenceGRCh38 38.1/142
Chromosome6
Position30724263
GeneTUBB
is asnp
is mentioned by
dbSNPrs587777357
ebirs587777357
HLIrs587777357
Exacrs587777357
Varsomers587777357
Maprs587777357
PheGenIrs587777357
hapmaprs587777357
1000 genomesrs587777357
hgdprs587777357
ensemblrs587777357
gopubmedrs587777357
geneviewrs587777357
scholarrs587777357
googlers587777357
pharmgkbrs587777357
gwascentralrs587777357
openSNPrs587777357
23andMers587777357
23andMe allrs587777357
SNP Nexus

SNPshotrs587777357
SNPdbers587777357
MSV3drs587777357
GWAS Ctlgrs587777357
Max Magnitude0
ClinVar
Risk rs587777357(A;A)
Alt rs587777357(A;A)
Reference rs587777357(G;G)
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.30692040G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000115020.2,