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rs751181600

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs751181600(G;T)
Make rs751181600(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position78164284
GeneWWOX
is asnp
is mentioned by
dbSNPrs751181600
dbSNP (classic)rs751181600
ClinGenrs751181600
ebirs751181600
HLIrs751181600
Exacrs751181600
Gnomadrs751181600
Varsomers751181600
LitVarrs751181600
Maprs751181600
PheGenIrs751181600
Biobankrs751181600
1000 genomesrs751181600
hgdprs751181600
ensemblrs751181600
geneviewrs751181600
scholarrs751181600
googlers751181600
pharmgkbrs751181600
gwascentralrs751181600
openSNPrs751181600
23andMers751181600
SNPshotrs751181600
SNPdbers751181600
MSV3drs751181600
GWAS Ctlgrs751181600
Max Magnitude0
ClinVar
Risk rs751181600(T;T)
Alt rs751181600(T;T)
Reference Rs751181600(G;G)
Significance Probable-Pathogenic
Disease Spinocerebellar ataxia
Variation info
Gene WWOX
CLNDBN Spinocerebellar ataxia, autosomal recessive 12
Reversed 0
HGVS NC_000016.9:g.78198181G>T
CLNSRC
CLNACC RCV000490293.1,