rs763162812
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs763162812(A;A) |
Make rs763162812(A;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 11 |
Position | 6616720 |
Gene | TPP1 |
is a | snp |
is | mentioned by |
dbSNP | rs763162812 |
dbSNP (classic) | rs763162812 |
ClinGen | rs763162812 |
ebi | rs763162812 |
HLI | rs763162812 |
Exac | rs763162812 |
Gnomad | rs763162812 |
Varsome | rs763162812 |
LitVar | rs763162812 |
Map | rs763162812 |
PheGenI | rs763162812 |
Biobank | rs763162812 |
1000 genomes | rs763162812 |
hgdp | rs763162812 |
ensembl | rs763162812 |
geneview | rs763162812 |
scholar | rs763162812 |
rs763162812 | |
pharmgkb | rs763162812 |
gwascentral | rs763162812 |
openSNP | rs763162812 |
23andMe | rs763162812 |
SNPshot | rs763162812 |
SNPdbe | rs763162812 |
MSV3d | rs763162812 |
GWAS Ctlg | rs763162812 |
Max Magnitude | 0 |
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, |