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rs532632165

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs532632165(C;G)
Make rs532632165(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position184357063
GeneCLCN2
is asnp
is mentioned by
dbSNPrs532632165
ebirs532632165
HLIrs532632165
Exacrs532632165
Varsomers532632165
Maprs532632165
PheGenIrs532632165
hapmaprs532632165
1000 genomesrs532632165
hgdprs532632165
ensemblrs532632165
gopubmedrs532632165
geneviewrs532632165
scholarrs532632165
googlers532632165
pharmgkbrs532632165
gwascentralrs532632165
openSNPrs532632165
23andMers532632165
23andMe allrs532632165
SNP Nexus

SNPshotrs532632165
SNPdbers532632165
MSV3drs532632165
GWAS Ctlgrs532632165
Max Magnitude0
ClinVar
Risk rs532632165(G;G)
Alt rs532632165(G;G)
Reference rs532632165(C;C)
Significance Pathogenic
Disease Leukoencephalopathy with ataxia
Variation info
Gene CLCN2
CLNDBN Leukoencephalopathy with ataxia
Reversed 0
HGVS NC_000003.11:g.184074851C>G
CLNSRC
CLNACC RCV000201818.1,