rs587778515
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs587778515(-;-) |
Make rs587778515(-;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 1 |
Position | 43338705 |
Gene | MPL |
is a | snp |
is | mentioned by |
dbSNP | rs587778515 |
dbSNP (classic) | rs587778515 |
ClinGen | rs587778515 |
ebi | rs587778515 |
HLI | rs587778515 |
Exac | rs587778515 |
Gnomad | rs587778515 |
Varsome | rs587778515 |
LitVar | rs587778515 |
Map | rs587778515 |
PheGenI | rs587778515 |
Biobank | rs587778515 |
1000 genomes | rs587778515 |
hgdp | rs587778515 |
ensembl | rs587778515 |
geneview | rs587778515 |
scholar | rs587778515 |
rs587778515 | |
pharmgkb | rs587778515 |
gwascentral | rs587778515 |
openSNP | rs587778515 |
23andMe | rs587778515 |
SNPshot | rs587778515 |
SNPdbe | rs587778515 |
MSV3d | rs587778515 |
GWAS Ctlg | rs587778515 |
Merged from | Rs886039426 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587778515(-;-) |
Alt | rs587778515(-;-) |
Reference | Rs587778515(T;T) |
Significance | Pathogenic |
Disease | not specified not provided |
Variation | info |
Gene | MPL |
CLNDBN | not specified not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.43804378delT |
CLNSRC | |
CLNACC | RCV000121537.1, RCV000255711.1, |