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rs796052407

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052407(C;T)
Make rs796052407(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position1759569
GeneCTSD
is asnp
is mentioned by
dbSNPrs796052407
ebirs796052407
HLIrs796052407
Exacrs796052407
Varsomers796052407
Maprs796052407
PheGenIrs796052407
hapmaprs796052407
1000 genomesrs796052407
hgdprs796052407
ensemblrs796052407
gopubmedrs796052407
geneviewrs796052407
scholarrs796052407
googlers796052407
pharmgkbrs796052407
gwascentralrs796052407
openSNPrs796052407
23andMers796052407
23andMe allrs796052407
SNP Nexus

SNPshotrs796052407
SNPdbers796052407
MSV3drs796052407
GWAS Ctlgrs796052407
Max Magnitude0
ClinVar
Risk rs796052407(T;T)
Alt rs796052407(T;T)
Reference rs796052407(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CTSD
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.1780799G>A
CLNSRC
CLNACC RCV000187320.1,