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rs763162812

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs763162812(A;A)
Make rs763162812(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position6616720
GeneTPP1
is asnp
is mentioned by
dbSNPrs763162812
ebirs763162812
HLIrs763162812
Exacrs763162812
Varsomers763162812
Maprs763162812
PheGenIrs763162812
hapmaprs763162812
1000 genomesrs763162812
hgdprs763162812
ensemblrs763162812
gopubmedrs763162812
geneviewrs763162812
scholarrs763162812
googlers763162812
pharmgkbrs763162812
gwascentralrs763162812
openSNPrs763162812
23andMers763162812
23andMe allrs763162812
SNP Nexus

SNPshotrs763162812
SNPdbers763162812
MSV3drs763162812
GWAS Ctlgrs763162812
Max Magnitude0
ClinVar
Risk rs763162812(A;A)
Alt rs763162812(A;A)
Reference rs763162812(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene TPP1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.6637951T>A
CLNSRC
CLNACC RCV000189773.1,