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rs796053444

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053444(C;T)
Make rs796053444(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position6614638
GeneTPP1
is asnp
is mentioned by
dbSNPrs796053444
ebirs796053444
HLIrs796053444
Exacrs796053444
Varsomers796053444
Maprs796053444
PheGenIrs796053444
hapmaprs796053444
1000 genomesrs796053444
hgdprs796053444
ensemblrs796053444
gopubmedrs796053444
geneviewrs796053444
scholarrs796053444
googlers796053444
pharmgkbrs796053444
gwascentralrs796053444
openSNPrs796053444
23andMers796053444
23andMe allrs796053444
SNP Nexus

SNPshotrs796053444
SNPdbers796053444
MSV3drs796053444
GWAS Ctlgrs796053444
Max Magnitude0
ClinVar
Risk rs796053444(T;T)
Alt rs796053444(T;T)
Reference rs796053444(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TPP1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.6635869G>A
CLNSRC
CLNACC RCV000189795.1,