rs752453717
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs752453717(C;C) |
Make rs752453717(C;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 43338725 |
Gene | MPL |
is a | snp |
is | mentioned by |
dbSNP | rs752453717 |
dbSNP (classic) | rs752453717 |
ClinGen | rs752453717 |
ebi | rs752453717 |
HLI | rs752453717 |
Exac | rs752453717 |
Gnomad | rs752453717 |
Varsome | rs752453717 |
LitVar | rs752453717 |
Map | rs752453717 |
PheGenI | rs752453717 |
Biobank | rs752453717 |
1000 genomes | rs752453717 |
hgdp | rs752453717 |
ensembl | rs752453717 |
geneview | rs752453717 |
scholar | rs752453717 |
rs752453717 | |
pharmgkb | rs752453717 |
gwascentral | rs752453717 |
openSNP | rs752453717 |
23andMe | rs752453717 |
SNPshot | rs752453717 |
SNPdbe | rs752453717 |
MSV3d | rs752453717 |
GWAS Ctlg | rs752453717 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs752453717(C;C) |
Alt | rs752453717(C;C) |
Reference | Rs752453717(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | MPL |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.43804396G>C |
CLNSRC | |
CLNACC | RCV000414099.1, |