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rs863225252

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863225252(-;-)
Make rs863225252(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position184355721
GeneCLCN2
is asnp
is mentioned by
dbSNPrs863225252
dbSNP (old)rs863225252
ClinGenrs863225252
ebirs863225252
HLIrs863225252
Exacrs863225252
Gnomadrs863225252
Varsomers863225252
Maprs863225252
PheGenIrs863225252
Biobankrs863225252
1000 genomesrs863225252
hgdprs863225252
ensemblrs863225252
gopubmedrs863225252
geneviewrs863225252
scholarrs863225252
googlers863225252
pharmgkbrs863225252
gwascentralrs863225252
openSNPrs863225252
23andMers863225252
23andMe allrs863225252
SNP Nexus

SNPshotrs863225252
SNPdbers863225252
MSV3drs863225252
GWAS Ctlgrs863225252
Max Magnitude0
ClinVar
Risk rs863225252(-;-)
Alt rs863225252(-;-)
Reference Rs863225252(T;T)
Significance Pathogenic
Disease Leukoencephalopathy with ataxia not provided
Variation info
Gene CLCN2
CLNDBN Leukoencephalopathy with ataxia not provided
Reversed 1
HGVS NC_000003.11:g.184073509delA
CLNSRC
CLNACC RCV000201805.1, RCV000486791.1,