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rs137852620

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852620(A;A)
Make rs137852620(A;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position36674080
GeneSLC1A3
is asnp
is mentioned by
dbSNPrs137852620
ebirs137852620
HLIrs137852620
Exacrs137852620
Varsomers137852620
Maprs137852620
PheGenIrs137852620
hapmaprs137852620
1000 genomesrs137852620
hgdprs137852620
ensemblrs137852620
gopubmedrs137852620
geneviewrs137852620
scholarrs137852620
googlers137852620
pharmgkbrs137852620
gwascentralrs137852620
openSNPrs137852620
23andMers137852620
23andMe allrs137852620
SNP Nexus

SNPshotrs137852620
SNPdbers137852620
MSV3drs137852620
GWAS Ctlgrs137852620
Max Magnitude0
OMIM600111
Desc
Variant0002
Relatedalso
ClinVar
Risk rs137852620(A;A)
Alt rs137852620(A;A)
Reference rs137852620(T;T)
Significance Pathogenic
Disease Episodic ataxia
Variation info
Gene SLC1A3
CLNDBN Episodic ataxia, type 6
Reversed 0
HGVS NC_000005.9:g.36674182T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010049.5,