rs886039426
From SNPedia
Merged into | rs587778515 |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs886039426(-;-) |
Make rs886039426(-;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 1 |
Position | 43338707 |
Gene | MPL |
is a | snp |
is | mentioned by |
dbSNP | rs886039426 |
dbSNP (classic) | rs886039426 |
ClinGen | rs886039426 |
ebi | rs886039426 |
HLI | rs886039426 |
Exac | rs886039426 |
Gnomad | rs886039426 |
Varsome | rs886039426 |
LitVar | rs886039426 |
Map | rs886039426 |
PheGenI | rs886039426 |
Biobank | rs886039426 |
1000 genomes | rs886039426 |
hgdp | rs886039426 |
ensembl | rs886039426 |
geneview | rs886039426 |
scholar | rs886039426 |
rs886039426 | |
pharmgkb | rs886039426 |
gwascentral | rs886039426 |
openSNP | rs886039426 |
23andMe | rs886039426 |
SNPshot | rs886039426 |
SNPdbe | rs886039426 |
MSV3d | rs886039426 |
GWAS Ctlg | rs886039426 |
Status | Merged into rs587778515 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | |
Alt | |
Reference | Rs886039426(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, |