rs759080581
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs759080581(A;A) |
Make rs759080581(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 11 |
Position | 6618809 |
Gene | TPP1 |
is a | snp |
is | mentioned by |
dbSNP | rs759080581 |
dbSNP (classic) | rs759080581 |
ClinGen | rs759080581 |
ebi | rs759080581 |
HLI | rs759080581 |
Exac | rs759080581 |
Gnomad | rs759080581 |
Varsome | rs759080581 |
LitVar | rs759080581 |
Map | rs759080581 |
PheGenI | rs759080581 |
Biobank | rs759080581 |
1000 genomes | rs759080581 |
hgdp | rs759080581 |
ensembl | rs759080581 |
geneview | rs759080581 |
scholar | rs759080581 |
rs759080581 | |
pharmgkb | rs759080581 |
gwascentral | rs759080581 |
openSNP | rs759080581 |
23andMe | rs759080581 |
SNPshot | rs759080581 |
SNPdbe | rs759080581 |
MSV3d | rs759080581 |
GWAS Ctlg | rs759080581 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs759080581(A;A) |
Alt | rs759080581(A;A) |
Reference | Rs759080581(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | TPP1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.6640040G>A |
CLNSRC | |
CLNACC | RCV000189754.2, |