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rs145966505

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs145966505(G;T)
Make rs145966505(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position6616332
GeneTPP1
is asnp
is mentioned by
dbSNPrs145966505
dbSNP (classic)rs145966505
ClinGenrs145966505
ebirs145966505
HLIrs145966505
Exacrs145966505
Gnomadrs145966505
Varsomers145966505
LitVarrs145966505
Maprs145966505
PheGenIrs145966505
Biobankrs145966505
1000 genomesrs145966505
hgdprs145966505
ensemblrs145966505
geneviewrs145966505
scholarrs145966505
googlers145966505
pharmgkbrs145966505
gwascentralrs145966505
openSNPrs145966505
23andMers145966505
SNPshotrs145966505
SNPdbers145966505
MSV3drs145966505
GWAS Ctlgrs145966505
Max Magnitude0
ClinVar
Risk rs145966505(T;T)
Alt rs145966505(T;T)
Reference Rs145966505(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TPP1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.6637563G>T
CLNSRC
CLNACC RCV000437106.1,