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rs376823689

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs376823689(A;A)
Make rs376823689(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position184352042
GeneCLCN2
is asnp
is mentioned by
dbSNPrs376823689
ebirs376823689
HLIrs376823689
Exacrs376823689
Varsomers376823689
Maprs376823689
PheGenIrs376823689
hapmaprs376823689
1000 genomesrs376823689
hgdprs376823689
ensemblrs376823689
gopubmedrs376823689
geneviewrs376823689
scholarrs376823689
googlers376823689
pharmgkbrs376823689
gwascentralrs376823689
openSNPrs376823689
23andMers376823689
23andMe allrs376823689
SNP Nexus

SNPshotrs376823689
SNPdbers376823689
MSV3drs376823689
GWAS Ctlgrs376823689
Max Magnitude0
ClinVar
Risk rs376823689(A;A)
Alt rs376823689(A;A)
Reference rs376823689(G;G)
Significance Pathogenic
Disease Leukoencephalopathy with ataxia
Variation info
Gene CLCN2
CLNDBN Leukoencephalopathy with ataxia
Reversed 0
HGVS NC_000003.11:g.184069830G>A
CLNSRC
CLNACC RCV000201824.1,