rs145966505
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs145966505(G;T) |
Make rs145966505(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 11 |
Position | 6616332 |
Gene | TPP1 |
is a | snp |
is | mentioned by |
dbSNP | rs145966505 |
dbSNP (classic) | rs145966505 |
ClinGen | rs145966505 |
ebi | rs145966505 |
HLI | rs145966505 |
Exac | rs145966505 |
Gnomad | rs145966505 |
Varsome | rs145966505 |
LitVar | rs145966505 |
Map | rs145966505 |
PheGenI | rs145966505 |
Biobank | rs145966505 |
1000 genomes | rs145966505 |
hgdp | rs145966505 |
ensembl | rs145966505 |
geneview | rs145966505 |
scholar | rs145966505 |
rs145966505 | |
pharmgkb | rs145966505 |
gwascentral | rs145966505 |
openSNP | rs145966505 |
23andMe | rs145966505 |
SNPshot | rs145966505 |
SNPdbe | rs145966505 |
MSV3d | rs145966505 |
GWAS Ctlg | rs145966505 |
Max Magnitude | 0 |
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, |