rs397516382
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs397516382(A;A) |
Make rs397516382(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 15 |
Position | 63042893 |
Gene | TPM1 |
is a | snp |
is | mentioned by |
dbSNP | rs397516382 |
dbSNP (classic) | rs397516382 |
ClinGen | rs397516382 |
ebi | rs397516382 |
HLI | rs397516382 |
Exac | rs397516382 |
Gnomad | rs397516382 |
Varsome | rs397516382 |
LitVar | rs397516382 |
Map | rs397516382 |
PheGenI | rs397516382 |
Biobank | rs397516382 |
1000 genomes | rs397516382 |
hgdp | rs397516382 |
ensembl | rs397516382 |
geneview | rs397516382 |
scholar | rs397516382 |
rs397516382 | |
pharmgkb | rs397516382 |
gwascentral | rs397516382 |
openSNP | rs397516382 |
23andMe | rs397516382 |
SNPshot | rs397516382 |
SNPdbe | rs397516382 |
MSV3d | rs397516382 |
GWAS Ctlg | rs397516382 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs397516382(A;A) |
Alt | rs397516382(A;A) |
Reference | Rs397516382(G;G) |
Significance | Probable-Pathogenic |
Disease | not specified not provided |
Variation | info |
Gene | TPM1 |
CLNDBN | not specified not provided |
Reversed | 0 |
HGVS | NC_000015.9:g.63335092G>A |
CLNSRC | Children's Hospital of Eastern Ontario |
CLNACC | RCV000036351.5, RCV000223842.1, |