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rs141242566

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs141242566(C;T)
Make rs141242566(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position184353722
GeneCLCN2
is asnp
is mentioned by
dbSNPrs141242566
ebirs141242566
HLIrs141242566
Exacrs141242566
Varsomers141242566
Maprs141242566
PheGenIrs141242566
hapmaprs141242566
1000 genomesrs141242566
hgdprs141242566
ensemblrs141242566
gopubmedrs141242566
geneviewrs141242566
scholarrs141242566
googlers141242566
pharmgkbrs141242566
gwascentralrs141242566
openSNPrs141242566
23andMers141242566
23andMe allrs141242566
SNP Nexus

SNPshotrs141242566
SNPdbers141242566
MSV3drs141242566
GWAS Ctlgrs141242566
Max Magnitude0
ClinVar
Risk rs141242566(A,T;A,T)
Alt rs141242566(A,T;A,T)
Reference rs141242566(C;C)
Significance Pathogenic
Disease Leukoencephalopathy with ataxia
Variation info
Gene CLCN2
CLNDBN Leukoencephalopathy with ataxia
Reversed 0
HGVS NC_000003.11:g.184071510C>T
CLNSRC
CLNACC RCV000201843.1,