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rs876657720

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876657720(-;-)
Make rs876657720(-;A)
Make rs876657720(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position23336234
GeneSACS
is asnp
is mentioned by
dbSNPrs876657720
ebirs876657720
HLIrs876657720
Exacrs876657720
Varsomers876657720
Maprs876657720
PheGenIrs876657720
hapmaprs876657720
1000 genomesrs876657720
hgdprs876657720
ensemblrs876657720
gopubmedrs876657720
geneviewrs876657720
scholarrs876657720
googlers876657720
pharmgkbrs876657720
gwascentralrs876657720
openSNPrs876657720
23andMers876657720
23andMe allrs876657720
SNP Nexus

SNPshotrs876657720
SNPdbers876657720
MSV3drs876657720
GWAS Ctlgrs876657720
Max Magnitude0
ClinVar
Risk rs876657720(A;A)
Alt rs876657720(A;A)
Reference rs876657720(;)
Significance Pathogenic
Disease Spastic ataxia Charlevoix-Saguenay type
Variation info
Gene SACS
CLNDBN Spastic ataxia Charlevoix-Saguenay type
Reversed 1
HGVS NC_000013.10:g.23910374dupT
CLNSRC
CLNACC RCV000214078.1,