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

rs587777324

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777324(A;A)
Make rs587777324(A;G)
ReferenceGRCh38 38.1/142
Chromosome6
Position3154458
GeneTUBB2A
is asnp
is mentioned by
dbSNPrs587777324
ebirs587777324
HLIrs587777324
Exacrs587777324
Varsomers587777324
Maprs587777324
PheGenIrs587777324
hapmaprs587777324
1000 genomesrs587777324
hgdprs587777324
ensemblrs587777324
gopubmedrs587777324
geneviewrs587777324
scholarrs587777324
googlers587777324
pharmgkbrs587777324
gwascentralrs587777324
openSNPrs587777324
23andMers587777324
23andMe allrs587777324
SNP Nexus

SNPshotrs587777324
SNPdbers587777324
MSV3drs587777324
GWAS Ctlgrs587777324
Max Magnitude0
ClinVar
Risk rs587777324(A;A)
Alt rs587777324(A;A)
Reference rs587777324(G;G)
Significance Pathogenic
Disease Cortical dysplasia not specified
Variation info
Gene TUBB2A
CLNDBN Cortical dysplasia, complex, with other brain malformations 5 not specified
Reversed 0
HGVS NC_000006.11:g.3154692G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000114959.2, RCV000202934.1,