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rs876657721

From SNPedia

Orientationminus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs876657721(-;-)
Make rs876657721(-;TT)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position23335333
GeneSACS
is asnp
is mentioned by
dbSNPrs876657721
ebirs876657721
HLIrs876657721
Exacrs876657721
Varsomers876657721
Maprs876657721
PheGenIrs876657721
hapmaprs876657721
1000 genomesrs876657721
hgdprs876657721
ensemblrs876657721
gopubmedrs876657721
geneviewrs876657721
scholarrs876657721
googlers876657721
pharmgkbrs876657721
gwascentralrs876657721
openSNPrs876657721
23andMers876657721
23andMe allrs876657721
SNP Nexus

SNPshotrs876657721
SNPdbers876657721
MSV3drs876657721
GWAS Ctlgrs876657721
Max Magnitude0
ClinVar
Risk rs876657721(;)
Alt rs876657721(;)
Reference rs876657721(TT;TT)
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.23909472_23909473delAA
CLNSRC
CLNACC RCV000218042.1,