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rs587777468

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587777468(C;G)
ReferenceGRCh38 38.1/142
Chromosome19
Position6495966
GeneTUBB4A
is asnp
is mentioned by
dbSNPrs587777468
ebirs587777468
HLIrs587777468
Exacrs587777468
Varsomers587777468
Maprs587777468
PheGenIrs587777468
hapmaprs587777468
1000 genomesrs587777468
hgdprs587777468
ensemblrs587777468
gopubmedrs587777468
geneviewrs587777468
scholarrs587777468
googlers587777468
pharmgkbrs587777468
gwascentralrs587777468
openSNPrs587777468
23andMers587777468
23andMe allrs587777468
SNP Nexus

SNPshotrs587777468
SNPdbers587777468
MSV3drs587777468
GWAS Ctlgrs587777468
Max Magnitude0
ClinVar
Risk rs587777468(G;G)
Alt rs587777468(G;G)
Reference rs587777468(C;C)
Significance Pathogenic
Disease Leukodystrophy
Variation info
Gene TUBB4A
CLNDBN Leukodystrophy, hypomyelinating, 6
Reversed 1
HGVS NC_000019.9:g.6495977G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000128410.3,