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rs587777355

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587777355(A;G)
Make rs587777355(G;G)
ReferenceGRCh38 38.1/142
Chromosome6
Position30723957
GeneTUBB
is asnp
is mentioned by
dbSNPrs587777355
ebirs587777355
HLIrs587777355
Exacrs587777355
Varsomers587777355
Maprs587777355
PheGenIrs587777355
hapmaprs587777355
1000 genomesrs587777355
hgdprs587777355
ensemblrs587777355
gopubmedrs587777355
geneviewrs587777355
scholarrs587777355
googlers587777355
pharmgkbrs587777355
gwascentralrs587777355
openSNPrs587777355
23andMers587777355
23andMe allrs587777355
SNP Nexus

SNPshotrs587777355
SNPdbers587777355
MSV3drs587777355
GWAS Ctlgrs587777355
Max Magnitude0
ClinVar
Risk rs587777355(G;G)
Alt rs587777355(G;G)
Reference rs587777355(A;A)
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.30691734A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000115018.2,