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rs763407972

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs763407972(C;T)
Make rs763407972(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position1754982
GeneCTSD
is asnp
is mentioned by
dbSNPrs763407972
ebirs763407972
HLIrs763407972
Exacrs763407972
Varsomers763407972
Maprs763407972
PheGenIrs763407972
hapmaprs763407972
1000 genomesrs763407972
hgdprs763407972
ensemblrs763407972
gopubmedrs763407972
geneviewrs763407972
scholarrs763407972
googlers763407972
pharmgkbrs763407972
gwascentralrs763407972
openSNPrs763407972
23andMers763407972
23andMe allrs763407972
SNP Nexus

SNPshotrs763407972
SNPdbers763407972
MSV3drs763407972
GWAS Ctlgrs763407972
Max Magnitude0
ClinVar
Risk rs763407972(T;T)
Alt rs763407972(T;T)
Reference rs763407972(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CTSD
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.1776212C>T
CLNSRC
CLNACC RCV000187314.1,