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rs796052400

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052400(C;G)
Make rs796052400(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position1759606
GeneCTSD
is asnp
is mentioned by
dbSNPrs796052400
ebirs796052400
HLIrs796052400
Exacrs796052400
Varsomers796052400
Maprs796052400
PheGenIrs796052400
hapmaprs796052400
1000 genomesrs796052400
hgdprs796052400
ensemblrs796052400
gopubmedrs796052400
geneviewrs796052400
scholarrs796052400
googlers796052400
pharmgkbrs796052400
gwascentralrs796052400
openSNPrs796052400
23andMers796052400
23andMe allrs796052400
SNP Nexus

SNPshotrs796052400
SNPdbers796052400
MSV3drs796052400
GWAS Ctlgrs796052400
Max Magnitude0
ClinVar
Risk rs796052400(G;G)
Alt rs796052400(G;G)
Reference rs796052400(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CTSD
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.1780836G>C
CLNSRC
CLNACC RCV000187307.1,