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rs767399782

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs767399782(C;T)
Make rs767399782(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position6495736
GeneTUBB4A
is asnp
is mentioned by
dbSNPrs767399782
ebirs767399782
HLIrs767399782
Exacrs767399782
Varsomers767399782
Maprs767399782
PheGenIrs767399782
hapmaprs767399782
1000 genomesrs767399782
hgdprs767399782
ensemblrs767399782
gopubmedrs767399782
geneviewrs767399782
scholarrs767399782
googlers767399782
pharmgkbrs767399782
gwascentralrs767399782
openSNPrs767399782
23andMers767399782
23andMe allrs767399782
SNP Nexus

SNPshotrs767399782
SNPdbers767399782
MSV3drs767399782
GWAS Ctlgrs767399782
Max Magnitude0
ClinVar
Risk rs767399782(A,T;A,T)
Alt rs767399782(A,T;A,T)
Reference rs767399782(C;C)
Significance Probable-Pathogenic
Disease Leukodystrophy
Variation info
Gene TUBB4A
CLNDBN Leukodystrophy, hypomyelinating, 6
Reversed 0
HGVS NC_000019.9:g.6495747C>T
CLNSRC
CLNACC RCV000199587.1,