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rs587784502

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587784502(C;T)
Make rs587784502(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position3225124
GeneTUBB2B
is asnp
is mentioned by
dbSNPrs587784502
ebirs587784502
HLIrs587784502
Exacrs587784502
Varsomers587784502
Maprs587784502
PheGenIrs587784502
hapmaprs587784502
1000 genomesrs587784502
hgdprs587784502
ensemblrs587784502
gopubmedrs587784502
geneviewrs587784502
scholarrs587784502
googlers587784502
pharmgkbrs587784502
gwascentralrs587784502
openSNPrs587784502
23andMers587784502
23andMe allrs587784502
SNP Nexus

SNPshotrs587784502
SNPdbers587784502
MSV3drs587784502
GWAS Ctlgrs587784502
Max Magnitude0
ClinVar
Risk rs587784502(T;T)
Alt rs587784502(T;T)
Reference rs587784502(C;C)
Significance Probable-Pathogenic
Disease Polymicrogyria
Variation info
Gene TUBB2B
CLNDBN Polymicrogyria, asymmetric
Reversed 1
HGVS NC_000006.11:g.3225358G>A
CLNSRC
CLNACC RCV000147845.1,