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rs202189057

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs202189057(A;T)
Make rs202189057(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position6617695
GeneTPP1
is asnp
is mentioned by
dbSNPrs202189057
ebirs202189057
HLIrs202189057
Exacrs202189057
Varsomers202189057
Maprs202189057
PheGenIrs202189057
hapmaprs202189057
1000 genomesrs202189057
hgdprs202189057
ensemblrs202189057
gopubmedrs202189057
geneviewrs202189057
scholarrs202189057
googlers202189057
pharmgkbrs202189057
gwascentralrs202189057
openSNPrs202189057
23andMers202189057
23andMe allrs202189057
SNP Nexus

SNPshotrs202189057
SNPdbers202189057
MSV3drs202189057
GWAS Ctlgrs202189057
Max Magnitude0
ClinVar
Risk rs202189057(T;T)
Alt rs202189057(T;T)
Reference Rs202189057(A;A)
Significance Pathogenic
Disease not provided Inborn genetic diseases
Variation info
Gene TPP1
CLNDBN not provided Inborn genetic diseases
Reversed 0
HGVS NC_000011.9:g.6638926A>T
CLNSRC
CLNACC RCV000189751.1, RCV000210549.1,