Have questions? Visit https://www.reddit.com/r/SNPedia

rs786204416

From SNPedia

Orientationminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs786204416(-;-)
Make rs786204416(-;CT)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position23333409
GeneSACS
is asnp
is mentioned by
dbSNPrs786204416
ebirs786204416
HLIrs786204416
Exacrs786204416
Varsomers786204416
Maprs786204416
PheGenIrs786204416
hapmaprs786204416
1000 genomesrs786204416
hgdprs786204416
ensemblrs786204416
gopubmedrs786204416
geneviewrs786204416
scholarrs786204416
googlers786204416
pharmgkbrs786204416
gwascentralrs786204416
openSNPrs786204416
23andMers786204416
23andMe allrs786204416
SNP Nexus

SNPshotrs786204416
SNPdbers786204416
MSV3drs786204416
GWAS Ctlgrs786204416
Max Magnitude0
ClinVar
Risk rs786204416(;)
Alt rs786204416(;)
Reference rs786204416(CT;CT)
Significance Probable-Pathogenic
Disease Spastic ataxia Charlevoix-Saguenay type
Variation info
Gene SACS
CLNDBN Spastic ataxia Charlevoix-Saguenay type
Reversed 1
HGVS NC_000013.10:g.23907548_23907549delAG
CLNSRC Counsyl
CLNACC RCV000168999.1,