rs397516487
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs397516487(C;G) |
Make rs397516487(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 63061781 |
Gene | TPM1 |
is a | snp |
is | mentioned by |
dbSNP | rs397516487 |
dbSNP (classic) | rs397516487 |
ClinGen | rs397516487 |
ebi | rs397516487 |
HLI | rs397516487 |
Exac | rs397516487 |
Gnomad | rs397516487 |
Varsome | rs397516487 |
LitVar | rs397516487 |
Map | rs397516487 |
PheGenI | rs397516487 |
Biobank | rs397516487 |
1000 genomes | rs397516487 |
hgdp | rs397516487 |
ensembl | rs397516487 |
geneview | rs397516487 |
scholar | rs397516487 |
rs397516487 | |
pharmgkb | rs397516487 |
gwascentral | rs397516487 |
openSNP | rs397516487 |
23andMe | rs397516487 |
SNPshot | rs397516487 |
SNPdbe | rs397516487 |
MSV3d | rs397516487 |
GWAS Ctlg | rs397516487 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs397516487(G;G) |
Alt | rs397516487(G;G) |
Reference | Rs397516487(C;C) |
Significance | Probable-Pathogenic |
Disease | not specified |
Variation | info |
Gene | TPM1 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000015.9:g.63353980C>G |
CLNSRC | ClinVar |
CLNACC | RCV000036630.3, |