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rs137852681

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852681(A;A)
Make rs137852681(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position184352810
GeneCLCN2
is asnp
is mentioned by
dbSNPrs137852681
ebirs137852681
HLIrs137852681
Exacrs137852681
Varsomers137852681
Maprs137852681
PheGenIrs137852681
hapmaprs137852681
1000 genomesrs137852681
hgdprs137852681
ensemblrs137852681
gopubmedrs137852681
geneviewrs137852681
scholarrs137852681
googlers137852681
pharmgkbrs137852681
gwascentralrs137852681
openSNPrs137852681
23andMers137852681
23andMe allrs137852681
SNP Nexus

SNPshotrs137852681
SNPdbers137852681
MSV3drs137852681
GWAS Ctlgrs137852681
Max Magnitude0
OMIM600570
Desc
Variant0003
Relatedalso
ClinVar
Risk rs137852681(A;A)
Alt rs137852681(A;A)
Reference rs137852681(G;G)
Significance Unknown
Disease Epilepsy Leukoencephalopathy with ataxia
Variation info
Gene CLCN2
CLNDBN Epilepsy, juvenile absence 2 Leukoencephalopathy with ataxia
Reversed 1
HGVS NC_000003.11:g.184070598C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009604.3, RCV000201807.1,