rs146249964
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;T) | 3 | Carrier of a congenital amegakaryocytic thrombocytopenia mutation |
(T;T) | 0 | common in clinvar |
Make rs146249964(A;A) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 1 |
Position | 43337929 |
Gene | MPL |
is a | snp |
is | mentioned by |
dbSNP | rs146249964 |
dbSNP (classic) | rs146249964 |
ClinGen | rs146249964 |
ebi | rs146249964 |
HLI | rs146249964 |
Exac | rs146249964 |
Gnomad | rs146249964 |
Varsome | rs146249964 |
LitVar | rs146249964 |
Map | rs146249964 |
PheGenI | rs146249964 |
Biobank | rs146249964 |
1000 genomes | rs146249964 |
hgdp | rs146249964 |
ensembl | rs146249964 |
geneview | rs146249964 |
scholar | rs146249964 |
rs146249964 | |
pharmgkb | rs146249964 |
gwascentral | rs146249964 |
openSNP | rs146249964 |
23andMe | rs146249964 |
SNPshot | rs146249964 |
SNPdbe | rs146249964 |
MSV3d | rs146249964 |
GWAS Ctlg | rs146249964 |
Max Magnitude | 3 |
aka c.79+2T>A
This variant in the thrombopoietin receptor-encoding gene, MPL, was reported in 2011 to be a founder mutation the Ashkenazi Jewish (AJ) population for CAMT (congenital amegakaryocytic thrombocytopenia), and the carrier frequency was estimated to be 1 in 75.[PMID 21489838]
ClinVar | |
---|---|
Risk | rs146249964(A;A) |
Alt | rs146249964(A;A) |
Reference | Rs146249964(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.43803600T>A |
CLNSRC | |
CLNACC | RCV000122423.1, RCV000254762.1, |